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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471310Generated: October 31, 2026

Dimethyl Sulfoxide → 8-(Tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-octanal

https://huagongshe.com/reaction/471310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant8-(tert-Butyldimethylsilyloxy)-2,2-dimethyloctan-1-olHCID 57989270—
SolventDichloromethaneHCID 6344—
Product8-(Tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-octanalHCID 86636755—

Reaction Steps

Oxalyl Chloride (5.9 mL) was added at −70° C. to a solution of dimethylsulfoxide (4.98 mL) in dry dichloromethane (60 mL) and the mixture stirred for 1 hour. 8-(tert-Butyldimethylsilyloxy)-2,2-dimethyloctan-1-ol (example 279, step b) (10.11 g), dissolved in dichloromethane (20 mL), was added dropwise and the mixture allowed to stir for 1 hour. Triethylamine (19.4 mL) was then added and stirring continued for 1 hour. The cooling bath was removed and the mixture allowed to warm to room temperature, at which point DCM (15 mL) was added. 1N HCl was added dropwise to dissolve the salts present in the reaction mixture and the layers separated. The aqueous layer was extracted with DCM (2×250 mL) then the combined organic layers were washed with saturated aqueous sodium carbonate (250 mL), dried over magnesium sulfate, filtered and concentrated under vacuum to give an orange liquid. The residue was filtered through a short plug of silica using diethyl ether as the eluent to afford 8-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-octanal as a yellow liquid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-bb248f287f7142aa9e71844df2d66a2c
Source noteuspto-grants-2014_01