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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837252Generated: November 2, 2026

Sodium borohydride → HCID 131724565, compound

https://huagongshe.com/reaction/1837252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131724564HCID 131724564—
SolventMethanolHCID 887—
ProductHCID 131724565HCID 13172456513.3%

Reaction Steps

2.4 g of 7α-{5-[(3,4,4,5,5,6,6,7,7,8,8,8-dodecafluor-oct-2-enyl)-methyl-amino]-pentyl}-11β-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one is dissolved in 15 ml of methanol and carefully mixed with 222 mg of sodium borohydride. After 15 minutes of stirring at room temperature, the batch is added to saturated common salt solution, extracted with methylene chloride, dried on magnesium sulfate and concentrated by evaporation in a vacuum. After the crude product is chromatographed on silica gel with ethyl acetate as an eluant, 319 mg of 7α-{5-[(3,4,4,5,5,6,6,7,7,8,8,8-dodecafluor-oct-2-enyl)-methyl-amino]-pentyl}-11β-fluor-estra-1,3,5(10)-triene-3,17β-diol is obtained as a foam, [α]D=+37° (c=0.5 in CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780855B2
Source datasetuspto-grants-2004_08
ORD IDord-68c00ec43d8f444f98595013a9a4902a
Source noteuspto-grants-2004_08