Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654914Generated: October 31, 2026

Acetic Anhydride → HCID 15723371, compound

https://huagongshe.com/reaction/654914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 19885953HCID 19885953—
CatalystPyridineHCID 1049—
ProductHCID 15723371HCID 15723371—

Reaction Steps

A solution of 4-(1-hydroxy-4-phenylbutyl)-2-trimethylsilylfuran (0.249 g., 0.862 mmol), acetic anhydride (1 ml, excess) and pyridine (3 to 4 drops, excess) was stirred at room temperature until no starting material remained (as monitored by TLC). The reaction mixture was then partitioned between ethyl ether and a 5% ammonium chloride solution. The organic portion was washed repeatedly with saturated sodium bicarbonate solution, twice with aqueous cupric sulfate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give a pale yellow oil (0.396 g). This material was further purified by flash chromatography (silica, 5% ethyl acetate/hexane) to give the desired acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134128
Source datasetuspto-grants-1992_07
ORD IDord-58dd659746294c1c96c31a140fac7d4e
Source noteuspto-grants-1992_07