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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47739Generated: October 28, 2026

HCID 2756026, compound → tert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamate

https://huagongshe.com/reaction/47739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2756026HCID 2756026—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Producttert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamateHCID 14212468100.7%

Reaction Steps

The process is performed as in Example 3, starting with 2.66 g of tert-butyl (1S)-1-benzyl-2-oxopropylcarbamate in 25 cm3 of ethanol, with 0.58 g of sodium borohydride. After 4 h 30 min at a temperature in the region of 20° C., the reaction mixture is worked up in an identical manner. 2.7 g of tert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamate are obtained in the form of a white solid melting at 125° C., as a mixture of the two diastereoisomers (70/30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699895B2
Source datasetuspto-grants-2004_03
ORD IDord-a16f5264168242eeb42d9d57d61e37da
Source noteuspto-grants-2004_03