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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866342Generated: October 29, 2026

Water → HCID 86735822, compound

https://huagongshe.com/reaction/866342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium borohydrideHCID 4148881—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22803980HCID 22803980—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86735822HCID 8673582210.9%

Reaction Steps

To 1-molar diborane-tetrahydrofuran complex (not stabilized with sodium borohydride, 157 ml) cooled in an ice bath, was added dropwise over about 25 minutes a solution of 1α,2α-epoxy-6β-methylsulfonyloxy-5α-cholestan-25-ol-3-one (20.0 g, 0.392 mole), in tetrahydrofuran (100 ml) with stirring under an atmosphere of nitrogen. After the addition was complete, the solution was stirred for about 25 minutes. Lithium borohydride (3.40 g, 0.155 mole) was added in 1 portion to the reaction mixture, with stirring. The suspension was stirred in an ice bath for about 6 hours and then stored in a refrigerator (ca. 3° C) overnight. Water (200 ml) was added cautiously to the reaction mixture cooled in an ice bath. An additional 200 ml of water was added to the turbid solution and the solution was extracted with methylene chloride. The layers were separated and the organic phase was washed successively with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate and filtered. Evaporation of the filtrate gave 22 g of 1α,25-dihydroxy-6β-methylsulfonyloxy-5α-cholestan-3-ol as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04098801
Source datasetuspto-grants-1978_07
ORD IDord-ce9c445036064cb69430af9d466a9028
Source noteuspto-grants-1978_07