Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595248Generated: October 29, 2026

Sodium borohydride → HCID 131734576, compound

https://huagongshe.com/reaction/595248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1522241-50-4HCID 96482004—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 131734576HCID 131734576—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (621 mg, 16.42 mmol) was added to a mixture of (R)-tert-butyl (4-chloro-3-oxobutan-2-yl)carbamate (910 mg, 4.10 mmol) in methanol (9 mL) at 0° C., and the mixture was stirred for one hour at 0° C. A few drops of acetic acid were added then the mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford tert-butyl ((2R)-4-chloro-3-hydroxybutan-2-yl)carbamate. 1H NMR (500 MHz, DMSO-d6) δ 6.65 (d, J=8.1 Hz, 1H), 5.24 (d, J=5.6 Hz, 1H), 3.58-3.53 (m, 1H), 3.50-3.44 (m, 2H), 3.44-3.34 (m, 1H), 1.36 (s, 9H), 0.99 (d, J=6.3, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-2c85c12eda7848878505f9c88efef5ce
Source noteuspto-grants-2016_01