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US4618700A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of a hydroxyphenylcarboxylate

Assignee: BASF Corp
•
Filing: 1984-12-12
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Granted: 1986-10-21
•
Expires: 2004-12-12
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Abstract

Abstract Pentaerythrityl tetrakis-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] is prepared by transesterifying a lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate with pentaerythritol in the presence of a basic catalyst, without addition of an inert solvent and in a 15 to 50% excess of lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate over the stoichiometric amount of 4 moles per 1 mole of pentaerythritol. An extremely good yield of pure crystalline product is obtained by the process of the invention.

Inventors

  • 👤 Erich Gubler
  • 👤 Max Siegrist

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 11:12
CPC Classifications
C; C07; C07C; C07C67/00; C07C67/03; C07C69/00; C07C69/66; C07C69/73; C07C69/732

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 56 words
A process for the preparation of pentaerythrityl tetrakis-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] by transesterifying a lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate with pentaerythritol, in the presence of a catalytic amount of a basic catalyst, which process comprises carrying out the transesterification with a 15 to 50% excess of lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate over the stoichiometric amount of 4 moles per 1 mole of pentaerythritol.
Claim 2
Dependent Claim 56 words
A process for the preparation of pentaerythrityl tetrakis-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] by transesterifying a lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate with pentaerythritol, in the presence of a catalytic amount of a basic catalyst, which process comprises carrying out the transesterification with a 15 to 50% excess of lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate over the stoichiometric amount of 4 moles per 1 mole of pentaerythritol.
Claim 3
Dependent Claim 30 words
A process according to claim 1, wherein a 25 to 35% excess of lower alkyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate over the stoichiometric amount of 4 moles per 1 mole of pentaerythritol is used.
Claim 4
Dependent Claim 11 words
A process according to claim 1, wherein lower alkyl is methyl.
Claim 5
Dependent Claim 23 words
A process according to claim 1, wherein the catalyst is used in an amount of 0.5 to 10 mol %, based on pentaerythritol.
Claim 6
Dependent Claim 27 words
A process according to claim 1, wherein lithium amide or dibutyltin oxide is used as catalyst in an amount of 1.0 to 6 mol.%, based on pentaerythritol.
Claim 7
Dependent Claim 13 words
A process according to claim 5, wherein lithium amide is used as catalyst.
Claim 8
Dependent Claim 21 words
A process according to claim 1, wherein the transesterification is carried out in the temperature range from 120° to 220° C.
Claim 9
Dependent Claim 21 words
A process according to claim 1, wherein the transesterification is carried out under a pressure of 30 mbar to 1 mbar.

References Cited (Backward Citations)

US3644482A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-10-20 1990-04-21 1990-10-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-10-20 1994-04-21 1994-10-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-10-20 1998-04-21 1998-10-21 $7700.00 Window Closed / Lapsed

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