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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486217Generated: October 25, 2026

Sodium borohydride → HCID 178476301, compound

https://huagongshe.com/reaction/1486217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDry ice ethyleneglycolHCID 86601574—
ReactantHCID 178476300HCID 178476300—
SolventEthanolHCID 702—
ProductHCID 178476301HCID 17847630153%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (ethylene glycol+dry ice) solution of 2-(trans-4-(1-(tert-butoxycarbonylamino)-3-oxopropyl)cyclohexyl)ethyl acetate (1.88 g, 5.5 mmol) in ethanol (90 mL) was added NaBH4 (0.212 g, 5.5 mmol). The mixture was stirred at −10˜15° C. for 10 min and 0° C. for 10 min, and then quenched by addition of saturated aqueous NH4Cl solution (30 mL) and brine (30 mL). After removal of the volatile by evaporation, the aqueous residue was extracted with EtOAc, dried over Na2SO4. Purification by flash column chromatography (eluent: 30% EtOAc in hexanes to 40%) gave the alcohol product (1.0 g, 53%). LC/MC: 366.1 (MNa)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422314B2
Source datasetuspto-grants-2016_08
ORD IDord-a1d9572169cb42218c691f0f2f162e02
Source noteuspto-grants-2016_08