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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289673Generated: October 27, 2026

Chlorosulfonyl isocyanate → 2,6-Bis(1-methylethyl)-4-nitrophenyl sulfamate

https://huagongshe.com/reaction/2289673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant2,6-Diisopropyl-4-nitrophenolHCID 10680603—
SolventTolueneHCID 1140—
Product2,6-Bis(1-methylethyl)-4-nitrophenyl sulfamateHCID 1869884560%

Reaction Steps

N-Chlorosulfonyl isocyanate (7.2 mL, 82.6 mmol) was added slowly to a warm solution of 2,6-bis(1-methylethyl)-4-nitrophenol (17.57 g, 78.7 mmol) in 400 mL toluene. The resulting solution was heated to reflux for 6 hours and then cooled to room temperature and concentrated to give a brown oil. Quenched with 200 g ice and extracted with 4×500 mL dichloromethane. The organic solution was dried over MgSO4, filtered, and concentrated to give a tan solid. Recrystallization from dichloromethane gave 14.18 g (60%) of the title compound as an off-white solid; mp 163-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093744
Source datasetuspto-grants-2000_07
ORD IDord-b2525d5950614c7c8d08f494e1e14117
Source noteuspto-grants-2000_07