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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333683Generated: October 27, 2026

Potassium;tri(butan-2-yl)boranuide → 3beta-Hydroxy-androstane-11,17-dione

https://huagongshe.com/reaction/333683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium;tri(butan-2-yl)boranuideHCID 4304157—
ReactantAndrostane-3,11,17-trioneHCID 66657133—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3beta-Hydroxy-androstane-11,17-dioneHCID 2196876499.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

K-SELECTRIDE® (potassium tri-sec-butylborohydride, 98.39 mL, 98.01 mmol, 1M solution in THF) is added to a solution of Compound 1.13 (33.0 g, 109.27 mmol) in THF (330 mL) over 15 minutes under an inert atmosphere at −78 ° C. and is stirred for about 3-4 h at −78 ° C. The reaction mixture is quenched with aqueous NaOH solution (2M, 70 mL). The crude reaction mixture is diluted with ethyl acetate (500 mL) and the organic layer is washed with water (3×75 mL), saturated brine solution (100 mL) and dried over MgSO4 (75 g). The solvent is removed under vacuum to afford 33 g of crude material. The crude product is subjected to acetylation without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883770B2
Source datasetuspto-grants-2014_11
ORD IDord-bc71fd852b374fd485a3d579acfd6eb9
Source noteuspto-grants-2014_11