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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 4-Chloro-2-fluoro-5-nitroaniline | HCID 13753061 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 4-Chloro-2-fluoro-5-nitrophenylisothiocyanate | HCID 14622954 | 95.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906281 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-484bcdc3f8a84eb6b7854448b3072b26 |
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| Source note | uspto-grants-1990_03 |
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