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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636289Generated: November 1, 2026

Acetic Anhydride → HCID 19350797, compound

https://huagongshe.com/reaction/1636289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 19350843HCID 19350843—
SolventPyridineHCID 1049—
ProductHCID 19350797HCID 19350797—

Reaction Conditions

Temperature5 °C

Reaction Steps

5-Benzyloxymethyl-1,4-oxathian-2-ol (3.46 g) was dissolved in pyridine (37 ml), and the solution was cooled to 5° C. Acetic anhydride (3.27 ml) was added dropwise thereto, and the solution was stirred at the same temperature for 4 hours to complete the reaction. After removing the solvent by evaporation under reduced pressure, the residue was azeotroped with toluene to completely remove pyridine to obtain pale brown syrup. The syrup was purified on a silica gel column (eluent: n-hexane/ethyl acetate=3/1) to provide the desired product (2.94 g) as colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034087
Source datasetuspto-grants-2000_03
ORD IDord-746ae9b69e764118943eb7244c635a6e
Source noteuspto-grants-2000_03