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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363866Generated: October 30, 2026

Triethylamine → HCID 66920960, compound

https://huagongshe.com/reaction/1363866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantBis(trimethylsilyl)methylamineHCID 10997564—
ReactantEthanol, 1-bromo-HCID 14202443—
SolventDichloromethaneHCID 6344—
ProductHCID 66920960HCID 6692096065%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 2.18 ml of chlorosulfonyl isocyanate in 10 ml of dichloromethane is added dropwise, at 0° C., a solution of 1.77 ml of bromoethanol in 10 ml of dichloromethane. The reaction medium is stirred for 10 minutes at 0° C. and then added dropwise to a solution of 4.38 grams of bis(trimethylsilyl)methylamine and 3.51 ml of triethylamine in 40 ml of dichloromethane at 0° C. After warming to 20° C. and stirring for 4 hours, the reaction mixture is cooled to 0° C. and 10.5 ml of triethylamine are then added dropwise. The reaction mixture is then stirred overnight at room temperature. It is then diluted with dichloromethane and washed 3 times with dilute hydrochloric acid. The organic phase is then washed once with saturated aqueous NaCl solution and then dried over sodium sulfate and concentrated under reduced pressure to give a white solid, 2-oxooxazolidine-3-sulfonic acid [bis(trimethylsilanyl)methyl]amide (65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07887824B2
Source datasetuspto-grants-2011_02
ORD IDord-3bef8fd6a3484fb88a7830e35b175cb2
Source noteuspto-grants-2011_02