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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451809Generated: October 30, 2026

Sodium borohydride → HCID 59383050, compound

https://huagongshe.com/reaction/451809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59382883HCID 59382883—
SolventEthanolHCID 702—
ProductHCID 59383050HCID 5938305099%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of (S)-methyl 2-(tert-butoxycarbonylamino)-3-(4,4-difluorocyclohexyl)propanoate (28.6 g, 0.089 mol) in EtOH (600 mL) at 0° C. was added NaBH4 (27.1 g, 0.713 mol) in portions while the temperature was maintained at 0-5° C. The mixture was stirred for 2-3 hr at rt and then evaporated. The residue was partitioned between water and EtOAc. The organic layer was washed with H2O and brine, dried over Na2SO4 and evaporated to give (S)-tert-butyl 1-(4,4-difluorocyclohexyl)-3-hydroxypropan-2-ylcarbamate (25.7 g, 99%), which was used in the next step without purification. 1H NMR (CDCl3, 400 MHz) δ 4.61 (d, J=7.6 Hz, 1H), 3.70 (m, 1H), 3.50 (m, 1H), 2.45-1.10 (m, 11H), 1.44 (s, 9H). MS ESI +ve m/z 295 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-bb8a5cbe39044ecf9f616b29264feeb3
Source noteuspto-grants-2013_07