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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant(5-Amino-2-bromophenyl)pentafluorosulfurHCID 86701290—
SolventTolueneHCID 1140—
Product1-Bromo-4-isocyanato-2-(pentafluoro-lambda6-sulfanyl)benzeneHCID 86701291—

Reaction Conditions

Temperature72 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937088B2
Source datasetuspto-grants-2015_01
ORD IDord-c57fb84d6d704e52b86bdd7fa8727068
Source noteuspto-grants-2015_01