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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973274Generated: October 25, 2026

Acetic Anhydride → 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester

https://huagongshe.com/reaction/973274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantTriphenylmethyl perchlorateHCID 10904004—
Reactant6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl esterHCID 86733276—
Product6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl esterHCID 53843942—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3.32 parts of 6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, 1.56 parts of triphenylmethyl perchlorate and 30 parts of acetic anhydride was heated at 100° C for 30 minutes. After cooling, the reaction mixture was poured into sodium bicarbonate solution and the resulting mixture was washed with water, dried and the ether was evaporated to give an oil which was chromatographed on silica gel using a 1:1 mixture of chloroform and light petroleum (b.p. 40°-60° C) for elution. This yielded 0.14 parts of 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, m.p. 130°-131.5° C (after crystallisation from light petroleum (b.p. 40°-60° C). This product was shown by spectral means to be the same as that prepared in Example 13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055654
Source datasetuspto-grants-1977_10
ORD IDord-33a39b919ffc48f0ac3ccfb647023bd4
Source noteuspto-grants-1977_10