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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935475Generated: November 3, 2026

Acetic Anhydride → HCID 54376764, compound

https://huagongshe.com/reaction/1935475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 401453HCID 401453—
SolventEthyl orthoformateHCID 31214—
ProductHCID 54376764HCID 5437676494%

Reaction Steps

0.5 ml of acetic anhydride was added to 3.8 g (14.9 mmol) of 2-amino-3-carboethoxy-5-ethyl-4,5,6,7-tetrahydrothieno-[3,2-c]pyridine in 40 ml of triethyl orthoformate, and the mixture was boiled under nitrogen and at reflux for 1 h. After the mixture had been decanted off from the insoluble black coating on the flask walls, it was then evaporated right down at 80° C. on a rotary evaporator. 3.5 g (94%) of crude product were isolated as a dark oil which is sufficiently pure for further reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387912B1
Source datasetuspto-grants-2002_05
ORD IDord-c8ed0477ea2742c3bacbc56cc6c68854
Source noteuspto-grants-2002_05