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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806999Generated: October 26, 2026

Dimethyl Sulfoxide → 5-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentanal

https://huagongshe.com/reaction/1806999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant5-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentan-1-olHCID 86640419—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentanalHCID 8664042094%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Step B To a solution of oxalyl chloride (0.1 mL, 1 mmol) (Aldrich) in dichloromethane (5 mL) at −78° C. was added the solution of dimethyl sulfoxide (0.16 mL, 2.2 mmol) in dichloromethane (1 mL) dropwise. After 5 mins, the solution of 5-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentan-1-ol (0.3 g, 1 mmol) in dichloromethane (1 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 15 min. Triethylamine (0.5 mL, 3.6 mmol) was added and the reaction mixture was slowly warmed up to room temperature and stirred at room temperature for 45 min. Then water was added. The organic layers were separated, and the aqueous layer was extracted with dichloromethane. The organic layers were combined, washed with 10% of HCl, saturated NaHCO3, brine, dried over MgSO4, and concentrated to give 5-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,3-dimethyl-pentanal as a yellow oil (Yield: 0.27 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-d90097fea00646d3a8d34a87b3d7f087
Source noteuspto-grants-2013_01