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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614406Generated: November 3, 2026

Acetic Anhydride → HCID 131717831, compound

https://huagongshe.com/reaction/1614406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131717832HCID 131717832—
SolventPyridineHCID 1049—
ProductHCID 131717831HCID 131717831—

Reaction Conditions

Temperature25 °C

Reaction Steps

For acetylation, 0.5 ml of acetic anhydride is added to a solution of 310 mg of the above-described alcohol in 2 ml of pyridine and stirred for 16 hours at 25° C. Then, it is concentrated by evaporation with adding toluene in a vacuum and the residue is chromatographed on silica gel. With hexane/1-5% of methyl-tert-butyl ether, 265 mg of 5-[(1E,3E)-(5RS)-5-acetoxy-1,3-tridecadienyl]-phenyl]-pentan-1-ol-diphenyl-tert-butylsilyl ether is obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196570
Source datasetuspto-grants-1993_03
ORD IDord-e72e7b95caa44ca09c1ae260594782c8
Source noteuspto-grants-1993_03