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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182889Generated: November 1, 2026

Sodium borohydride → HCID 68781188, compound

https://huagongshe.com/reaction/1182889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68729360HCID 68729360—
SolventMethanolHCID 887—
ProductHCID 68781188HCID 6878118898.8%

Reaction Steps

To a suspension of 4α-acetoxyandrost-5-ene-3,17-dione (600 mg) in MeOH (20 ml) at 0° C., NaBH4 (70 mg) was added. The mixture was warmed and stirred for 1 h at RT. The solution was neutralized by addition of 5% NaH2PO4 and the organic solvent was evaporated. The residue was taken up in H2O and extracted with DCM. The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated to dryness. The resulting 4α-acetoxyandrost-5-ene-3,17β-diol (600 mg) was obtained as a 3α:3β mixture and used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664210B2
Source datasetuspto-grants-2014_03
ORD IDord-798e3e137d3143a28ed0bdcf90e511fa
Source noteuspto-grants-2014_03