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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605767Generated: November 2, 2026

Acetic Anhydride → HCID 20465612, compound

https://huagongshe.com/reaction/1605767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
Reactant2-(5-Hydroxypentyl)cyclopentan-1-oneHCID 20465518—
Reactant2-(5-Hydroxypentyl)cyclopentanone 2-(5-acetoxypentyl)-cyclopentanoneHCID 86732937—
ProductHCID 20465612HCID 20465612—

Reaction Steps

A solution of 400 g. (2.04 moles) of a mixture of 2-(5-hydroxypentyl)cyclopentanone and 2-(5-acetoxypentyl)cyclopentanone (Example 55) and 4.0 g. of p-toluenesulfonic acid monohydrate in 11. l. of acetic anhydride is refluxed acetic a rate to maintain a steady distillation of accetic acid from the reaction through a helix -packed fractionation column. The reaction is continued with the addition of acetic anhydride to maintain a constant volume until complete conversion of starting materials to product is evident. The mixture is cooled and partitioned between 2 l. of hexane and 3 l. of cold water containing solid sodium bicarbonate to maintain a neutral pH. The organic phase is washed with saturated brine, dried (MgSO4), and evaporated to yield 452 g. of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950406
Source datasetuspto-grants-1976_04
ORD IDord-a8bcc23e0e154d2283ea2345a83fc5e5
Source noteuspto-grants-1976_04