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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921484Generated: October 31, 2026

Acetic Anhydride → HCID 117774505, compound

https://huagongshe.com/reaction/921484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 53632406HCID 53632406—
CatalystZinc bromideHCID 10421208—
ProductHCID 117774505HCID 117774505—

Reaction Steps

ZnBr2 (3.0 g, 13.4 mmol) was added to a solution of acetic anhydride (30 mL) and 4-methyl-tricyclo[6.2.1.0(2,7)]undec-4-ene (10.0 g, 62 mmol) and then heated under reflux. After 2 hours at reflux the mixture was cooled then poured into dilute NH4OH (6%) and extracted with diethyl ether. The organic phase was washed with saturated NaHCO3, then brine, dried over Na2SO4, filtered and the solvents removed in vacuo. The crude ketone (9.3 g orange oil) was further purified by bulb to bulb distillation 0.1 mbar at 120° C. gave the desired ketone, 5.4 g as a mixture of isomers (7:6:16:21:16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273268B2
Source datasetuspto-grants-2016_03
ORD IDord-57e38804233741e298fa6fb7b9e71ecd
Source noteuspto-grants-2016_03