Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725184Generated: November 2, 2026

Sodium borohydride → (1S,3aS,5S,7aR)-1-acetoxymethyl-7a-methylperhydroinden-3a,5-diol

https://huagongshe.com/reaction/725184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(1S,3aS,7aR)-1-acetoxymethyl-3a-hydroxy-7a-methyl-5-perhydroindenoneHCID 22880912—
SolventMethanolHCID 887—
Product(1S,3aS,5S,7aR)-1-acetoxymethyl-7a-methylperhydroinden-3a,5-diolHCID 5705411843.2%

Reaction Steps

To a solution of 5.00 g of (1S,3aS,7aR)-1-acetoxymethyl-3a-hydroxy-7a-methyl-5-perhydroindenone (see Prepn. 3) in 50 ml of methanol cooled at 0° C., 0.77 g of NaBH4 were added and the mixture was stirred for 1 hr. It was then diluted with 10 ml of 5% aqueous NaH2PO4.H2O, concentrated in vacuo and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by flash-chromatography (SiO2) with n-hexane/chloroform/acetone 4:3:3 as the eluant to give 2.18 g of (1S,3aS,5S,7aR)-1-acetoxymethyl-7a-methylperhydroinden-3a,5-diol as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705531
Source datasetuspto-grants-1998_01
ORD IDord-2b8071db366f4eb699edd624b33f3e93
Source noteuspto-grants-1998_01