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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475845Generated: October 26, 2026

Sodium borohydride → 3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol

https://huagongshe.com/reaction/1475845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanoneHCID 57565772—
SolventTetrahydrofuranHCID 8028—
Product3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanolHCID 5756574569.6%

Reaction Steps

3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanone (5.11 g, 14.5 mmol) (WO 2006063281) was dissolved in tetrahydrofuran (120 mL). Sodium borohydride (548 mg, 14.5 mmol) was added and the reaction was stirred overnight at room temperature. The reaction was quenched with water and saturated aqueous sodium bicarbonate and stirred for 20 min until the bubbling ceased. The reaction mixture was diluted with ether and the aqueous layer was extracted with ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuo to give 3-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol (3.58 g, 69.6%) as a clear oil. Partial 1H NMR indicated a ˜3.5:1 mix of cis-trans isomers. (CDCl3, δ ppm, key peaks are 4.08 (quintet, J=7.42, 0.78H) and 4.34 (quintet, J=6.83, 0.22H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018384B2
Source datasetuspto-grants-2015_04
ORD IDord-d56bf87d490244b7a8c659262d1035e9
Source noteuspto-grants-2015_04