HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4196Generated: October 25, 2026
Dichloromethane → N-[2-[(4-Fluorophenyl)thio]ethyl]-N-(1-methylethyl)carbamic acid phenyl ester
https://huagongshe.com/reaction/4196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 2-(4-Fluorophenylthio]ethyl-1-methyl-ethanamine | HCID 86740885 | — |
| Product | N-[2-[(4-Fluorophenyl)thio]ethyl]-N-(1-methylethyl)carbamic acid phenyl ester | HCID 13655160 | — |
Reaction Steps
To a solution of 38.5 g (0.15 mole) of N-[2-(4-fluorophenylthio]ethyl-1-methyl-ethanamine and 15.5 g (0.15 mole) of triethylamine in 300 ml of methylene chloride which was cooled in an ice bath was added dropwise with stirring a solution of 23.5 g (0.15 mole) of phenyl chloroformate in 100 ml of methylene chloride over a 15 minute period. The resulting solution was stirred overnight at room temperature and extracted with 5% aqueous sodium hydroxide. The chloroform layer was dried and filtered and evaporated to give an oil residue which crystallized to a white solid. A portion of the solid was triturated with isopropyl ether and the mixture cooled under refrigeration. The solid was collected by filtration and dried in vacuo overnight at 80° C. White crystalline product, m.p. 53°-58° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04724235 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-5d2d6d1bd4bb4895b8b561dcce002bb1 |
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| Source note | uspto-grants-1988_02 |
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