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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594978Generated: October 31, 2026

3-Hydroxybenzaldehyde → 3-(t-Butyldimethylsilyloxy)benzaldehyde

https://huagongshe.com/reaction/594978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
Product3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 11207111100%

Reaction Steps

tert-butyldimethylsilyl chloride (3.7 g, 1.5 eq) was added portionwise to a solution of 3-hydroxybenzaldehyde (2.0 g, 16 mmol), triethylamine (3.4 mL, 1.5 eq) and dimethylaminopyridine (50 mg, 0.025 eq) in DCM (100 mL). After stirring for 2 h at rt, water was added. The aqueous phase was extracted with DCM, the combined organic phases dried over sodium sulfate and concentrated in vacuo to afford 3-((tert-butyldimethylsilyl)oxy)benzaldehyde (3.6 g, 16 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242987B2
Source datasetuspto-grants-2016_01
ORD IDord-1d02d6ffce9d4a1a93dcaa2d89d00e04
Source noteuspto-grants-2016_01