HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905425Generated: November 1, 2026
Hydrochloric Acid → 3,4-Difluorophenyl Isothiocyanate
https://huagongshe.com/reaction/1905425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3,4-Difluoroaniline | HCID 77469 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3,4-Difluorophenyl Isothiocyanate | HCID 2758331 | 70.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04843070 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-49d3f7faedf94f53863a5c12ceede17a |
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| Source note | uspto-grants-1989_06 |
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