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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786161Generated: October 31, 2026

Triethylamine → 1,1-Dimethylethyl N-[1-[2-[(methylsulfonyl)oxy]ethyl]cyclopropyl]carbamate

https://huagongshe.com/reaction/1786161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,1-Dimethylethyl N-[1-(2-hydroxyethyl)cyclopropyl]carbamateHCID 12993139—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethylethyl N-[1-[2-[(methylsulfonyl)oxy]ethyl]cyclopropyl]carbamateHCID 1299314087%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 6.472 g (32.16 mmol) of tert-butyl 1-(2-hydroxyethyl)cyclopropylcarbamate in 61 ml of anhydrous dichloromethane was added 12.79 ml (91 mmol) of anhydrous triethylamine. The resulting mixture is cooled at −20° C. Then 3.54 ml (45.66 mmol) of mesyl chloride in 11 ml of anhydrous dichloromethane was added. The resulting mixture was stirred at room temperature for 2 h. The mixture was poured into ice-water and the organic layer was washed with saturated aqueous sodium chloride, dried over sodium sulfate and evaporated. The crude product was triturated with petroleum ether and filtered to give 7.82 g of pure product as an orange solid. Mp: 88-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507743B2
Source datasetuspto-grants-2009_03
ORD IDord-0187f9bd4d8442db85d80f59adc4af0b
Source noteuspto-grants-2009_03