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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287458Generated: October 30, 2026

Acetic Anhydride → HCID 54487648, compound

https://huagongshe.com/reaction/2287458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2,7,8-Trimethyl-2-(beta-carboxy-ethyl)-6-hydroxychromanHCID 133098—
SolventPyridineHCID 1049—
ProductHCID 54487648HCID 54487648—

Reaction Steps

Racemic 2,7,8-Trimethyl-2-(β-carboxyethyl)-6-hydroxy chroman (500 mg) (see Example 11) was dissolved in pyridine (20 mL) at room temperature, and acetic anhydride (10 mL) was added. The solution was maintained at room temperature for 5 hours, solvent was removed under vacuum, methanol (4×10 mL) was added and then removed under reduced pressure. The residual oil was dissolved in ethyl acetate (150 mL) and the organic phase was washed with water (50 mL), aqueous HCl (1 N, 50 mL) and water (50 mL), then dried over sodium sulfate. Solvent was then removed, and the residual oily material was purified on a silica gel column with hexane/ethyl acetate (1:1). The desired product crystallized from acetone/hexane, m.p. 105-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083982
Source datasetuspto-grants-2000_07
ORD IDord-7260e3201e75466c9598b5bb648831d5
Source noteuspto-grants-2000_07