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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384052Generated: November 1, 2026

Hydrochloric Acid → 3-((Tert-butyldimethylsilyl)oxy)propanal

https://huagongshe.com/reaction/1384052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant3-[(Tert-butyldimethylsilyl)oxy]propan-1-olHCID 4077791—
SolventDichloromethaneHCID 6344—
Product3-((Tert-butyldimethylsilyl)oxy)propanalHCID 3662392—

Reaction Conditions

Temperature-78 °C

Reaction Steps

DMSO (24 mmol) is added to oxalyl chloride (11 mmol) in 40 mL of CH2Cl2 cooled to −78° C. After 15 minutes, alcohol 46 (10 mmol) is added. After an additional 15 minutes, triethylamine (50 mmol) is added. The mixture is allowed to warm to 0° C. and then poured into 0.1 M HCl (100 mL). The phases are separated, and the aqueous phase is extracted with ethyl acetate (2×100 mL). The organic phases are washed with water (100 mL), dried over anhydrous MgSO4, and concentrated in vacuo. The mixture is purified by flash chromatography to give the product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258360B1
Source datasetuspto-grants-2001_07
ORD IDord-a99d66bef24646e7b36a58d2187dcce7
Source noteuspto-grants-2001_07