HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428414Generated: November 3, 2026
Triethylamine → 1-Bromo-4-isocyanato-2-(pentafluoro-lambda6-sulfanyl)benzene
https://huagongshe.com/reaction/1428414
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | (5-Amino-2-bromophenyl)pentafluorosulfur | HCID 86701290 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Bromo-4-isocyanato-2-(pentafluoro-lambda6-sulfanyl)benzene | HCID 86701291 | — |
Reaction Steps
To a solution of 4-bromo-3-(pentafluoro-λ6-sulfanyl)aniline (2.36 g, 7.92 mmol, 1.0 eq) in toluene (70 mL) was added triphosgene (1.57 g, 5.3 mmol, 0.67 eq) under N2 at room temperature. Triethylamine (1.31 mL, 9.37 mmol, 1.2 eq) was added dropwise by syringe. The mixture was stirred at 72° C. (oil bath) for 2 hrs. TLC (hexane/EtOAc=2/1, UV) indicated that starting material was consumed. The mixture was allowed to cool to room temperature. Hexane (100 mL) was added. The precipitate was removed by filtration, washed with hexane (30 mL). The combined filtrate was concentrated by evaporator in vacuo at 70° C. for 40 min to afford crude 1-bromo-4-isocyanato-2-(pentafluoro-λ6-sulfanyl)benzene as a brown liquid which was used immediately for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937088B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-c57fb84d6d704e52b86bdd7fa8727068 |
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| Source note | uspto-grants-2015_01 |
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