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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764725Generated: November 3, 2026

Ethyl chloroformate → HCID 54490095, compound

https://huagongshe.com/reaction/1764725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 53947568HCID 53947568—
SolventBenzeneHCID 241—
ProductHCID 54490095HCID 54490095—

Reaction Steps

50 ml of ethyl chloroformate were added dropwise over 5 minutes at 20° C. under nitrogen to a mixture of 7.9 g of N,N-dimethyl-2-nitro-6,7-dihydro [5H] benzocycloheptene-7-methanamine in 50 ml of benzene and the mixture was refluxed for 2 hours and then evaporated to dryness. The residue was extracted with ether and the ether phase was washed with N hydrochloric acid solution and then with water, was dried and distilled to dryness under reduced pressure to obtain 9 g of ethyl methyl-[(2-nitro-6,7-dihydro [5H] benzocycloheptene-7-yl) methyl]-carbamate in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04117164
Source datasetuspto-grants-1978_09
ORD IDord-7b034f3419574216b3a1cef357be521d
Source noteuspto-grants-1978_09