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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292374Generated: October 31, 2026

Chlorosulfonyl isocyanate → HCID 86742712, compound

https://huagongshe.com/reaction/2292374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactantbenzyl N-[(3S)-2-oxoazetidin-3-yl]carbamateHCID 12834624—
ReactantHCID 21277154HCID 21277154—
SolventEthyl AcetateHCID 8857—
ProductHCID 86742712HCID 86742712—

Reaction Steps

To a suspension of 3.9 g (17.8 mmol) of (S)-(2-oxo-3-azetidinyl)carbamic acid, phenylmethyl ester in 30 ml of ethyl acetate was added 2.5 g (17.8 mmol) of chlorosulfonyl isocyanate. The reaction mixture was stirred for one hour at room temperature and a solution of 7.14 g (17.8 mmol) of 1-[3,4-bis[(trimethylsilyl)oxy]phenyl]-3-(trimethylsilyl)-2-imidazolidinone in 30 ml of ethyl acetate was added dropwise. After stirring overnight at room temperature, the mixture was washed with brine, dried over sodium sulfate and evaporated in vacuo; yield: 8.46 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04801705
Source datasetuspto-grants-1989_01
ORD IDord-e586551ab007452687957cdac4d9d8ed
Source noteuspto-grants-1989_01