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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 5-Amino-4-cyano-3-ethoxyisothiazole | HCID 21396819 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenyl (4-cyano-3-ethoxy-5-isothiazolyl)carbamate | HCID 54236272 | 40.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04059433 |
|---|
| Source dataset | uspto-grants-1977_11 |
|---|
| ORD ID | ord-7b59006193a942c883d9024a01ef2f8b |
|---|
| Source note | uspto-grants-1977_11 |
|---|