HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382739Generated: October 30, 2026
Triethylamine → 2,3,4-Trifluorophenyl isothiocyanate
https://huagongshe.com/reaction/1382739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | N,N-diethyl-1-ethanaminium N-(2,3,4-trifluorophenyl)carbamodithioate | HCID 16413959 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,3,4-Trifluorophenyl isothiocyanate | HCID 2760791 | 78.3% |
Reaction Steps
Triethylammonium N-(2,3,4-trifluorophenyl)dithiocarbamate (92.0 g) and triethylamine (31.5 g) were added to chloroform (360 ml) and thereto ethyl chlorocarbonate (33.8 g) was added dropwise at 2°-6° C. with stirring over a period of 1 hour. The mixture was stirred for 10 minutes and washed with 3N hydrochloric acid and then with water. The organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica-gel column chromatography (Silica gel 60, 230-400 mesh, made by Merck Co., 220 g, eluent: hexane) under medium pressure, followed by distillation under reduced pressure to give the title compound (42.0 g) as colorless liquid, b.p.: 96°-97° C./17 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04808584 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-fb954e5e34894d5193e689d39daf86c3 |
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| Source note | uspto-grants-1989_02 |
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