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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289683Generated: October 30, 2026

Chlorosulfonyl isocyanate → HCID 18698847, compound

https://huagongshe.com/reaction/2289683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant4-(Tert-butyl-dimethyl-silanyloxy)-2,6-diisopropylphenolHCID 18698837—
SolventTolueneHCID 1140—
ProductHCID 18698847HCID 1869884741.6%

Reaction Steps

N-Chlorosulfonyl isocyanate (3.43 mL, 39.4 mmol) was added to a warm solution of 4-(tert-butyl-dimethyl-silanyloxy)-2,6-diisopropylphenol (11.59 g, 37.6 mmol) in 400 mL toluene. The resulting solution was heated to reflux for 6 hours and then cooled to room temperature and stirred overnight. The reaction was concentrated in vacuo, and the residue was quenched with ice water and extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered, and concentrated to give an orange oil. Chromatography on silica gel gave 6.06 g of 4-(tert-butyl-dimethyl-silanyloxy)-2,6-diisopropylphenyl sulfamate as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093744
Source datasetuspto-grants-2000_07
ORD IDord-affc43a758644be1830c83964d674abc
Source noteuspto-grants-2000_07