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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44722Generated: October 29, 2026

Hydrogen Peroxide → 3-(1-{[Tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propan-1-ol

https://huagongshe.com/reaction/44722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
Reactant[(1-Allylcyclohexyl)oxy](tert-butyl)dimethylsilaneHCID 57457814—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-(1-{[Tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propan-1-olHCID 5745781579%

Reaction Steps

A solution of borane in tetrahydrofuran (1 M, 15.7 mL, 15.7 mmol) was added to a solution of [(1-allylcyclohexyl)oxy](tert-butyl)dimethylsilane (8.00 g, 31.4 mmol) in tetrahydrofuran. After 2 h, water (5 mL) was added dropwise, followed by 3 M NaOH (6 mL), followed by dropwise addition of 30% aqueous hydrogen peroxide (6 mL). The mixture was stirred at rt for 1 h, then was diluted with diethyl ether (100 mL) and water (70 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (2×35 mL). The combined organic layers were washed with brine (90 mL), dried over MgSO4, filtered, and concentrated to yield a colorless oil that was purified using HPFC (silica gel, gradient elution with 2-30% ethyl acetate/hexanes) to afford pure 3-(1-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propan-1-ol (6.80 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-9222fa0966a749208fd54afd711cac12
Source noteuspto-grants-2013_09