Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304789Generated: October 31, 2026

Hydrochloric Acid → Benzyl ((2R,3S)-4-chloro-3-hydroxy-1-(phenylthio)butan-2-yl)carbamate

https://huagongshe.com/reaction/2304789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum isopropoxideHCID 11143—
ReactantZ-D-Phe chloromethyl ketoneHCID 10808734—
SolventIsopropanolHCID 3776—
ProductBenzyl ((2R,3S)-4-chloro-3-hydroxy-1-(phenylthio)butan-2-yl)carbamateHCID 995103180%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 2.15 g aluminium isopropoxide in 35 ml of isopropanol were added 3.64 g of benzyl [3-chloro-2-oxo-(R)-1-(phenylthiomethyl)-propyl]-carbamate and the mixture was stirred at 50° C./400mbar for 4 hours. The mixture was cooled to 0° C., the pH was adjusted to 1 by adding hydrochloric acid and the isopropanol was evaporated. The residue was partitioned between water and dichloromethane and the organic layer was evaporated. The residue was chromatographed on silica to give 2.9 g (80%) of pure benzyl (1R, 2S)-[3-chloro-2-hydroxy-1-(phenylthiomethyl)-propyl]-carbamate. IR (KBr): 3360 br (NH, OH), 1690 s (C═O), 1540 s (amide II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437134B1
Source datasetuspto-grants-2002_08
ORD IDord-106029996b244de398fb9a9adfe762ed
Source noteuspto-grants-2002_08