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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232546Generated: October 31, 2026

Sodium borohydride → 8-t-Butyl-3-hydroxy-1-oxaspiro(4,5)decane

https://huagongshe.com/reaction/232546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant8-t-Butyl-1-oxaspiro(4,5)decane-3-oneHCID 15182818—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
Product8-t-Butyl-3-hydroxy-1-oxaspiro(4,5)decaneHCID 1904015798,679.102%

Reaction Steps

To an ice cooled solution of 8-t-butyl-1-oxaspiro(4,5)decane-3-one (44.1 g, 0.21 mmol) in methanol (300 ml) was added sodium borohydride (10.8 g, 0.285 mol) in portions. After the evolution of hydrogen ceased the cooling bath was removed and the mixture was stirred at room temperature over night. The solvent was evaporated in vacuo and the residue was taken up in toluene/diluted hydrochloric acid. The organic layer was washed twice with water (200 ml), dried (MgSO4) and evaporated in vacuo to yield a colourless oil (44 g) which was recrystallised from light petroleum. 30 g of colourless crystals were obtained which melted at 82°-84° C. TLC and NMR-analysis indicated a single diastereoisomer only (cis).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591741
Source datasetuspto-grants-1997_01
ORD IDord-95b7c425cf0146ccb9296b6db133875d
Source noteuspto-grants-1997_01