Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850146Generated: October 30, 2026

Sodium borohydride → 1429182-35-3

https://huagongshe.com/reaction/1850146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-butyl N-(2-methyl-3-oxobutan-2-yl)carbamateHCID 22973790—
SolventMethanolHCID 887—
Product1429182-35-3HCID 8673018188.9%

Reaction Steps

To a solution of tert-butyl 2-methyl-3-oxobutan-2-ylcarbamate (2.36 g, 11.73 mmol) in MeOH (30 mL) at 0° C. was added portion wise NaBH4 (0.887 g, 23.45 mmol). Cold bath was removed and the reaction was stirred for 1 hour. HCl solution (1 M, 0.2 mL) was then added cautiously to quench the reaction. The reaction mixture was then concentrated and diluted with EtOAc (50 mL) and water (10 mL). The phases were separated and the aqueous layer was extracted with EtOAc (2×20 mL). The combined organics were then dried (Na2SO4) and concentrated under reduced pressure. The residue was purified via silica gel flash chromatography (10-50% EtOAc-Hexanes) to afford the desired product as a white solid (2.12 g). LCMS m/z 204.1 (M+H)+, Rt 0.69 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957068B2
Source datasetuspto-grants-2015_02
ORD IDord-97bc390e53234788b002dc154cb3976c
Source noteuspto-grants-2015_02