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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755131Generated: November 3, 2026

Methanesulfonyl chloride → HCID 23449785, compound

https://huagongshe.com/reaction/1755131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 23449785HCID 23449785—

Reaction Steps

(2-Hydroxyethyl)methylcarbamic acid 1,1-dimethylethyl ester (350 mg, 2.0 mmol) was dissolved in pyridine (2 ml). Mesyl chloride (0.229 ml, 2.1 mmol) was added at room temperature, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was diluted with methylene chloride, and the organic layer was washed with a saturated aqueous sodium bicarbonate solution, dried over MgSO4 and concentrated under reduced pressure to give methanesulfonic acid 2-(tert-butoxycarbonyl-methyl-amino)-ethyl ester. This was used in the next reaction without complete purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-8ed846b3b4514e90b5ef499c1ddde3f4
Source noteuspto-grants-2015_10