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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107559Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 22941134, compound

https://huagongshe.com/reaction/1107559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 53689600HCID 53689600—
SolventDichloromethaneHCID 6344—
ProductHCID 22941134HCID 22941134100.2%

Reaction Steps

DMSO (1.6 g, 21 mmol) was added to oxalyl chloride in CH2Cl2 (7.4 mL of 2 M solution, 14.8 mmole) at -78° C. The (-)-(trans)-2-(2,3-dihydrobenzofuran-4-yl)-cyclopropylmethanol (2.0 g, 10.5 mmol) in CH2Cl2 (15 mL) was added. The mixture was stirred for 20 min and then triethylamine (4.24 g, 42 mmol) was added. The mixture was warmed to room temperature and stirred for 30 min. The mixture was diluted with CH2Cl2 and washed with water, 1N HCl, and then 1N NaOH. The organic layer was dried and concentrated in vacuo to give the aldehyde product (1.98 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060506
Source datasetuspto-grants-2000_05
ORD IDord-defea4aae3f34e8aa344c8cf957971ed
Source noteuspto-grants-2000_05