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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982313Generated: October 29, 2026

Acetic Anhydride → HCID 20067450, compound

https://huagongshe.com/reaction/982313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 20067453HCID 20067453—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 20067450HCID 20067450—

Reaction Steps

3.4 g of 8-amino-7-chloro-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine in 50 ml of methylene chloride was treated with 4 ml of acetic anhydride followed by addition of 10 mg. of 4-dimethylaminopyridine. The resulting mixture was stirred at room temperature for 2 hours, and the solvent was removed in vacuo. The residue was stirred with a mixture of ether and sodium bicarbonate solution for 1 hour. The ether layer was separated, dried over sodium sulfate and evaporated in vacuo. The resulting crude product of this example (3.1 g) was used in the following step B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996202
Source datasetuspto-grants-1991_02
ORD IDord-234d0d8de5c9401ca23ceff74b6beb1f
Source noteuspto-grants-1991_02