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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837812Generated: November 1, 2026

Acetic Anhydride → Alpha-Tocopherol Acetate

https://huagongshe.com/reaction/1837812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsophytolHCID 10453—
ReactantTrimethylhydroquinoneHCID 12785—
ReactantBorateHCID 26574—
ProductAlpha-Tocopherol AcetateHCID 8647292%

Reaction Steps

EP 0 784 042 claimed hydrogen bis(oxalato)borate as protic acid catalyst for the Friedel-Crafts condensation of trimethylhydroquinone with isophytol and the acylation of phenols, for example tocopherol. In an example the acylation of tocopherol is described. For this, tocopherol was charged into a flask together with acetic anhydride and hydrogen bis(oxalato)borate and the reaction mixture was heated to reflux for one hour under an argon atmosphere. The initial molar ratio of acetic anhydride/tocopherol was greater than 1.1 mol/mol and the borate concentration was approximately 0.5 mol %, based on tocopherol. After concentration on a rotary evaporator, tocopherol acetate was obtained in a purity of 87% at a yield of 92%. This batch process has the disadvantage that both yield and purity are still not satisfactorily high. In addition, carrying out the reaction in an argon atmosphere is associated with high costs for industrial production.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784303B2
Source datasetuspto-grants-2004_08
ORD IDord-bff61d4b7a65495d8cd169531af4a7cb
Source noteuspto-grants-2004_08