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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287627Generated: November 1, 2026

Chloride → 3-((Tert-butyldimethylsilyl)oxy)propanal

https://huagongshe.com/reaction/2287627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant3-[(Tert-butyldimethylsilyl)oxy]propan-1-olHCID 4077791—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—

Reaction Steps

To a solution of anhydrous dimethylsulfoxide (0.05 mole) in anhydrous methylene chloride (100 ml) cooled to 0° C. under nitrogen with stirring is added a solution of oxalyl chloride (0.05 mole) in anhydrous methylene chloride (100 ml). After stirring for 15 minutes, a solution of 1-tert-Butyldimethylsilyloxy-3-hydroxypropane (0.04 mole) inmethylene chloride (150 ml) is added over a period of 30 minutes. Then the reaction is quenched by adding triethyl amine (1 mole) slowly. The reaction mixture is diluted with ethyl acetate (200 ml), washed with water (75 ml), brine (75 ml), dried and concentrated. The product is used as such in the subsequent condensation step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06084082
Source datasetuspto-grants-2000_07
ORD IDord-59e1f88ee0c84ce8ab6bdffeb37fccb6
Source noteuspto-grants-2000_07