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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484551Generated: October 31, 2026

Acetic Anhydride → 142034-81-9

https://huagongshe.com/reaction/484551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67747384HCID 67747384—
SolventSodium HydroxideHCID 14798—
Product142034-81-9HCID 15049039278.8%

Reaction Steps

To a cooled solution of trans-2-carboxymethoxy-cyclohexyl ammonium chloride (1.048 g, 5 mmoles) in 2N NaOH (5 ml), there were added under stirring first 1N NaOH (1 ml) and then acetic anhydride (0.102 g, 1 mmol). When the reaction of anhydride was completed and a homogeneous solution was obtained, the same amount of 1N NaOH and acetic anhydride as above was added four times. After the addition of the last portion the reaction mixture was stirred for 30 minutes, the solution was acidified to pH 2 and extracted with ethyl acetate (5×20 ml). The organic extracts were dried with MgSO4, the drying agent was filtered off and the filtrate was evaporated under reduced pressure. The residue was recrystallized from a mixture of chloroform/n-hexane. Thus, there were obtained 0.60 g (56%) of the title compound, melting point 141°-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231216
Source datasetuspto-grants-1993_07
ORD IDord-7bf474be29824fc6b0a9a3d97dcb6ff5
Source noteuspto-grants-1993_07