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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164708Generated: October 30, 2026

Triethylamine → 4-Chloro-2-fluoro-5-nitrophenylisothiocyanate

https://huagongshe.com/reaction/1164708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThiophosgeneHCID 10040—
Reactant4-Chloro-2-fluoro-5-nitroanilineHCID 13753061—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
Product4-Chloro-2-fluoro-5-nitrophenylisothiocyanateHCID 1462295495.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.), stirring mixture of 12.0 g (0.0630 mole) of 4-chloro-2-fluoro-5-nitroaniline in 100 mL of methylene chloride was added dropwise 7.3 g (0.063 mole) of thiophosgene. While maintaining a temperature of 0° C., 13.2 g (0.130 mole) of triethylamine was added dropwise to the mixture. After complete addition, the mixture was allowed to warm to room temperature and stir for approximately 18 hours. The solvent was evaporated under reduced pressure leaving a residue. This residue was stirred in a mixture of ethyl acetate and n-heptane (30:70). The insoluble amine hydrochloride salts were removed by filtration. The filtrate was evaporated under reduced pressure to yield 14.0 g of 4-chloro-2-fluoro-5-nitrophenylisothiocyanate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906281
Source datasetuspto-grants-1990_03
ORD IDord-484bcdc3f8a84eb6b7854448b3072b26
Source noteuspto-grants-1990_03