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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534083Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 86644155, compound

https://huagongshe.com/reaction/534083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67486253HCID 67486253—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventChlorineHCID 24526—
ProductHCID 86644155HCID 86644155110.4%

Reaction Steps

A solution of methylsulfinylmethane (20.6 ml, 289 mmol) in CH2 Cl2 (260 mL) at −60° C., was added dropwise to a 2M solution of oxalyl dichloride (15.2 ml, 174 mmol) in CH2Cl2 (80 mL). The mixture was stirred for 20 minutes and then a solution of ((2S,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decane-2-yl)methanol (31.3 g, 145 mmol) in CH2Cl2 (80 mL) was added dropwise. The mixture was stirred for 10 minutes and then triethylamine (101 ml, 724 mmol) was slowly added. The reaction mixture was warmed to ambient temperature and water was added. When the mixture became clear, it was extracted with CH2Cl2, dried over sodium sulfate, filtered and concentrated to afford crude ((2R,3S)-3-(methoxymethyl)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde (34.3 g, 96.2% yield, 87% pure) which was taken on to next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-3dccb769a1674022b867e491cacdae67
Source noteuspto-grants-2014_10