Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061055Generated: November 1, 2026

Ethyl Acetate → Benzyl 1-mercapto-2-methylpropan-2-ylcarbamate

https://huagongshe.com/reaction/2061055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantS-2-(Benzyloxycarbonylamino)-2-methylpropyl ethanethioateHCID 24787377—
SolventMethanolHCID 887—
ProductBenzyl 1-mercapto-2-methylpropan-2-ylcarbamateHCID 59614731—

Reaction Steps

A solution of S-2-(Benzyloxycarbonylamino)-2-methylpropyl ethanethioate (4.75 g, 16.9 mmol) in methanol (35 mL) was mixed with a 5 N sodium hydroxide solution (3 equiv, 50 mL, 50.7 mmol) and stirred at RT for 15 min. TLC (20% ethyl acetate in hexanes) analysis of reaction mixture indicated all the starting material was consumed. The organic solvent was removed under reduced pressure and the resulting aqueous solution was made acidic (˜pH 3) with 6 N HCl (9 mL) while cooled in an ice bath. The aqueous suspension was extracted with ethyl acetate (3×100 mL) and the combined organic layer dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give benzyl 1-mercapto-2-methylpropan-2-ylcarbamate as a pale yellow oil, 4.6 g. This material was used without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278482B2
Source datasetuspto-grants-2012_10
ORD IDord-b91cce98774c44f3b71ce7ffb8309174
Source noteuspto-grants-2012_10