Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846448Generated: October 25, 2026

4-Pyrrolidinopyridine → Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-

https://huagongshe.com/reaction/846448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyrrolidinopyridineHCID 75567—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant3-(Hydroxymethyl)benzaldehydeHCID 13131455—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductBenzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-HCID 10883279—

Reaction Steps

To a solution of 3-hydroxymethylbenzaldehyde (step 1) (3 g) in methylene chloride (15 mL) and triethylamine (4.1 mL) was slowly added t-butylchlorodiphenylsilane (8 mL). Finally, a few mgs of 4-pyrrolidinopyridine was added as a catalyst. The reaction mixture was stirred overnight at room temperature The solution was quenched with 25% ammonium acetate and extracted with ethyl acetate, which was washed with brine (2x), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography, using 4% ethyl acetate in hexane afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05136034
Source datasetuspto-grants-1992_08
ORD IDord-70b674dde4cd4a08bed0f79876742ad5
Source noteuspto-grants-1992_08