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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41139Generated: October 26, 2026

Sodium borohydride → (3-(2-((Triisopropylsilyl)oxy)ethyl)phenyl)methanol

https://huagongshe.com/reaction/41139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(2-((Triisopropylsilyl)oxy)ethyl)benzaldehydeHCID 54757655—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3-(2-((Triisopropylsilyl)oxy)ethyl)phenyl)methanolHCID 5475765699%

Reaction Steps

Sodium borohydride (0.062 g, 1.63 mmol) was added to a mixture of 14 (0.500 g, 1.63 mmol) in tetrahydrofuran (4 mL) and water (0.25 mL). The reaction mixture was heated to reflux temperature for 2 h. After cooling, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue so obtained was dried under high vacuum to afford the desired compound as colorless oil. Yield: 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530520B2
Source datasetuspto-grants-2013_09
ORD IDord-a870e9c963144b58968ae1ff49882552
Source noteuspto-grants-2013_09