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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609116Generated: October 30, 2026

Sodium borohydride → HCID 4983340, compound

https://huagongshe.com/reaction/1609116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22990221HCID 22990221—
SolventMethanolHCID 887—
ProductHCID 4983340HCID 4983340—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4.17 g (17.1 mmol) of methyl [3,5,5,8,8-pentamethyl(5,6,7,8-tetrahydronaphthalen-2-yl] ketone (Compound 10) in methanol at 0° C. was portionwise added 0.77 g (20.4 mmol) of sodium borohydride and the resulting suspension stirred at 0° C. for 4 hours. Solvent was removed in-vacuo and the resulting :solid taken-up in water, acidified using 1N HCl, and extracted three times with ether. The ether extracts were washed with water, brine and dried (MgSO4). The solvent was removed in-vacuo and resulting residue purified using flash chromatography (SiO2, 10% ethyl acetate in hexanes) to give a single isomer: the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399586
Source datasetuspto-grants-1995_03
ORD IDord-4ecc95b7fe0a42e683b9ba126278af0d
Source noteuspto-grants-1995_03