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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221406Generated: October 30, 2026

Triethylamine → 1-(3-(Benzyloxycarbonylamino)phenyl)-2-(tert-butyldimethylsilyloxy)ethyl methanesulfonate

https://huagongshe.com/reaction/221406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl 3-(2-(tert-butyldimethylsilyloxy)-1-hydroxyethyl)phenylcarbamateHCID 67329796—
SolventDichloromethaneHCID 6344—
Product1-(3-(Benzyloxycarbonylamino)phenyl)-2-(tert-butyldimethylsilyloxy)ethyl methanesulfonateHCID 86656264—

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl 3-(2-(tert-butyldimethylsilyloxy)-1-hydroxyethyl)phenylcarbamate (4 g) was dissolved in dry DCM (80 mL) and cooled to 0° C. under an argon atmosphere. Triethylamine (5 g) was added, followed by mesyl chloride (3.42 g) added drop-wise over a period of 2 hours. The reaction temp was maintained at 0° C. for further 2 hours. The reaction was quenched by addition of water, extracted into DCM and concentrated under vacuum at a temperature below 25° C. The crude product (3.5 g) was unstable and was used for next step as soon as possible.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207167B2
Source datasetuspto-grants-2012_06
ORD IDord-49811530307a4023ae613f30825e3c5f
Source noteuspto-grants-2012_06