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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905425Generated: November 1, 2026

Hydrochloric Acid → 3,4-Difluorophenyl Isothiocyanate

https://huagongshe.com/reaction/1905425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3,4-DifluoroanilineHCID 77469—
SolventChloroformHCID 6212—
Product3,4-Difluorophenyl IsothiocyanateHCID 275833170.2%

Reaction Steps

3,4-Difluoroaniline (600 g) and 1410 g of triethylamine were mixed and, with ice cooling and stirring, 389 g of carbon disulfide was dropped in during 2.5 hours. The mixture was stirred at the same temperature for 2 hours more whereupon crystals gradually appeared. The mixture was gradually warmed up to the room temperature, stirred for 2 hours, and kept in a refrigerator for two nights. Chloroform (2 liters) was added to the reaction mixture in which crystals were solidified, the mixture was stirred to make it suspended, and ethyl chloroformate was dropped in at 10° C. (inner temperature) during 2 hours. The mixture was stirred 3.5 hours more at room temperature. After the reaction, the reaction solution was poured over into ice water, the mixture was made weakly acidic with concentrated hydrochloric acid, and the chloroform layer was collected. This was washed with water, dried and concentrated and the residue was purified by a column chromatography (n-hexane/silica gel) to give 558.6 g of 3,4-difluorophenyl isothiocyanate in colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843070
Source datasetuspto-grants-1989_06
ORD IDord-49d3f7faedf94f53863a5c12ceede17a
Source noteuspto-grants-1989_06