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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439322Generated: November 1, 2026

Phenyl chloroformate → Phenyl (4-cyano-3-ethoxy-5-isothiazolyl)carbamate

https://huagongshe.com/reaction/1439322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant5-Amino-4-cyano-3-ethoxyisothiazoleHCID 21396819—
SolventTolueneHCID 1140—
ProductPhenyl (4-cyano-3-ethoxy-5-isothiazolyl)carbamateHCID 5423627240.5%

Reaction Steps

A solution of 16.6 g of 5-amino-4-cyano-3-ethoxyisothiazole and 30.7 g of phenyl chloroformate in 100 ml of toluene under nitrogen atmosphere was stirred and heated at 100° for about 16 hours. After this time, thin-layer chromatography indicated that the reaction was 50% complete. An additional 15 ml of phenyl chloroformate was added and heating (100°) continued for an additional 24 hours; at this time thin-layer chromatography indicated 80% reaction. After an additional 6 hours, 90% reaction was indicated. The mixture was allowed to cool to 5° and filtered. The solid filter cake was washed with toluene and recrystallized from acetic acid, then ethanol, to give 11.5 g of phenyl (4-cyano-3-ethoxy-5-isothiazolyl)carbamate, m.p. 252°-253°. The nmr spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04059433
Source datasetuspto-grants-1977_11
ORD IDord-7b59006193a942c883d9024a01ef2f8b
Source noteuspto-grants-1977_11