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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276269Generated: October 30, 2026

Methanesulfonyl chloride → HCID 59113179, compound

https://huagongshe.com/reaction/276269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantbenzyl ((2R,3R)-3-(tert-butoxy)-1-hydroxybutan-2-yl)carbamateHCID 59113072—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 59113179HCID 59113179100.7%

Reaction Steps

To a solution of (1R,2R)-N-(benzyloxycarbonyl)-1-(hydroxymethyl)-2-(tert-butoxy)propanamine (1.6 g, 5.4 mmol) in anh. pyridine (30 mL) at 4° C. was added methanesulfonyl chloride (0.75 mL, 9.7 mmol) dropwise. The reaction was stirred for 5.5 h, then was diluted with EtOAc (200 mL) and washed with a 1N HCl solution (4×200 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to yield (1R,2R)-N-(benzyloxycarbonyl)-1-(methanesulfonyloxymethyl)-2-(tert-butoxy)propanamine as an oil (2.03 g, 100%): TLC (25% EtOAc/hex) Rf0.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-64048efeedb04542a5227f6c22ac3205
Source noteuspto-grants-2002_03