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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366908Generated: October 30, 2026

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

https://huagongshe.com/reaction/366908

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-(phenylsulfanyl)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./ 400 mbar 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 numberUS06130348
Source datasetuspto-grants-2000_10
ORD IDord-da1f0146ade84064a14ab3983f3b8ee3
Source noteuspto-grants-2000_10