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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35721Generated: October 26, 2026

Dimethyl Sulfoxide → 3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanal

https://huagongshe.com/reaction/35721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(S)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanolHCID 10082693—
SolventTriethylamineHCID 8471—
Product3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanalHCID 10443866—

Reaction Steps

To 56.3 g. of oxalyl chloride in 300 ml. of dry methylene chloride cooled to -60° C. and under a nitrogen atmosphere was added dropwise 74.81 g. of dimethylsulfoxide in 100 ml. of dry methylene chloride. After 15 minutes 92.0 g. of 3-(S)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanol in 250 ml. of the same solvent was added dropwise. After 30 minutes 206.1 g. of triethylamine was added to -60° C. followed by the removal of the cooling bath. The reaction was stirred at room temperature for 1.5 hours, and was then poured into water and extracted with methylene chloride. The extracts were washed with 2.5% hydrochloric, a saturated sodium bicarbonate solution, water and a brine solution, and then dried over magnesium sulfate. The solvent was removed and the residue dissolved in ether and rewashed and dried as before. Removal of the ether gave 90.9 g. of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767743
Source datasetuspto-grants-1988_08
ORD IDord-154a74fe8a0c4d619de5a5dbe7a96915
Source noteuspto-grants-1988_08