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US4233245A
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Preparation of tris(hydroxymethyl)aminomethane
Assignee: Societe Chimique de la Grande Paroisse Azote et Produits Chimiques
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Filing: 1979-01-25
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Granted: 1980-11-11
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Expires: 1999-01-25
Abstract
Abstract Tris(hydroxymethyl)aminomethane, an intermediate of organic synthesis, in ystalline form is made by formylation followed by hydrogenation. Nitromethane and formaldehyde in a molar ratio on the order of 1:3 are reacted in a concentrated alcohol medium made up of a 2 to 5% mixture of methylene chloride in methanol, in the presence of 1 to 10 milliequivalents per mole of nitromethane of a solid base catalyst selected from sodium or potassium, with agitation for a period between 3 and 36 hours at a temperature below 50° C.
Inventors
- 👤 Jean Bourguignon
- 👤 Marcel-Xavier Sion
- 👤 Michel Moreau
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-29 10:02
CPC Classifications
C; C07; C07C; C07C213/00; C07C213/02
Claims Analysis
Total Claims: 9
Claim 1
Independent Claim
162 words
in a process of preparing tris(hydroxymethyl)aminomethane in crystalline form separated directly by cooling of the reaction medium, the process comprising formylation followed by hydrogenation, the improvement wherein nitromethane and formaldehyde, in polyoxymethylene or solid form, are reacted to effect said formylation in a molar ratio on the order of 1:3 in a concentrated alcohol medium of 2 to 5% mixture of methylene chloride in methanol, in the presence of 1 to 10 milliequivalents per mole of nitromethane of a basic catalyst in solid form, selected from sodium or potassium, with agitation for a period between 2 and 36 hours at a temperature below 55° C.; and the product of the formylation is acidified with concentrated acid to a pH between 4.5 and 5.5, the resultant acidified nitroalcohol is diluted with methanol containing 2 to 5% methylene chloride, and is then catalytically hydrogenated on Raney nickel at a hydrogen pressure of 30 to 60 bars at a temperature of 40 to 47° C.
Claim 2
Dependent Claim
162 words
in a process of preparing tris(hydroxymethyl)aminomethane in crystalline form separated directly by cooling of the reaction medium, the process comprising formylation followed by hydrogenation, the improvement wherein nitromethane and formaldehyde, in polyoxymethylene or solid form, are reacted to effect said formylation in a molar ratio on the order of 1:3 in a concentrated alcohol medium of 2 to 5% mixture of methylene chloride in methanol, in the presence of 1 to 10 milliequivalents per mole of nitromethane of a basic catalyst in solid form, selected from sodium or potassium, with agitation for a period between 2 and 36 hours at a temperature below 55° C.; and the product of the formylation is acidified with concentrated acid to a pH between 4.5 and 5.5, the resultant acidified nitroalcohol is diluted with methanol containing 2 to 5% methylene chloride, and is then catalytically hydrogenated on Raney nickel at a hydrogen pressure of 30 to 60 bars at a temperature of 40 to 47° C.
Claim 3
Dependent Claim
31 words
Process of preparing tris(hydroxymethyl)aminomethane according to claim 1 wherein the weight of the Raney nickel is between 5 and 25% in relation to the weight of the nitroalcohol to be reduced.
Claim 4
Dependent Claim
16 words
Process of preparing tris(hydroxymethyl)aminomethane accordance to claim 1 wherein the dilution methanol contains 2.5% methylene chloride.
Claim 5
Dependent Claim
138 words
In a process of preparing tris (hydroxymethyl) aminomethane in crystalline form separated directly by cooling of the reaction medium, by formylation followed by hydrogenation, the improvement comprising formylating nitromethane by reaction with formaldehyde, in polyoxymethylene or solid form, in concentrated methanol containing 2-5% methylene chloride, in the presence of 1 to 10 milliequivalents of sodium in solid form per mole of nitromethane, the mole ratio of nitromethane to formaldehyde being on the order of 1:3; acidifying the resultant product of the formylation reaction with concentrated hydrochloric acid to a pH between 4.5 and 5.5, diluting the resultant acidified nitroalcohol with methanol containing 2 to 5% methylene chloride, and then catalytically hydrogenating using Raney nickel at a hydrogen pressure between 30 and 60 bars and a temperature between 40° and 47° C., whereby tris(hydroxymethyl)aminomethane is precipitated in crystalline form.
Claim 6
Dependent Claim
138 words
In a process of preparing tris (hydroxymethyl) aminomethane in crystalline form separated directly by cooling of the reaction medium, by formylation followed by hydrogenation, the improvement comprising formylating nitromethane by reaction with formaldehyde, in polyoxymethylene or solid form, in concentrated methanol containing 2-5% methylene chloride, in the presence of 1 to 10 milliequivalents of sodium in solid form per mole of nitromethane, the mole ratio of nitromethane to formaldehyde being on the order of 1:3; acidifying the resultant product of the formylation reaction with concentrated hydrochloric acid to a pH between 4.5 and 5.5, diluting the resultant acidified nitroalcohol with methanol containing 2 to 5% methylene chloride, and then catalytically hydrogenating using Raney nickel at a hydrogen pressure between 30 and 60 bars and a temperature between 40° and 47° C., whereby tris(hydroxymethyl)aminomethane is precipitated in crystalline form.
Claim 7
Dependent Claim
29 words
Process in accordance with claim 4, wherein the weight of the Raney nickel is between 5 and 25% in relation to the weight of the nitroalcohol to be reduced.
Claim 8
Dependent Claim
14 words
Process in accordance with claim 4, wherein the dilution methanol contains 2.5% methylene chloride.
Claim 9
Dependent Claim
82 words
Process of preparing tris(hydroxymethyl)aminoethane according to any of claims 1 to 6 wherein a first batch of the final product in crystalline form is separated directly by cooling of the reaction medium free of hydrogenation catalyst; then a second batch, of generally the same purity as the first, is obtained after separation of the first batch followed by concentration of the mother liquors to an oily residue and extraction from the oily residue by a 30% mixture of methanol in methylene chloride.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1983-11-11 | 1984-05-12 | 1984-11-11 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1987-11-11 | 1988-05-12 | 1988-11-11 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1991-11-11 | 1992-05-12 | 1992-11-11 | $7700.00 | Window Closed / Lapsed |