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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842939Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 86586557, compound

https://huagongshe.com/reaction/842939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69468650HCID 69468650—
SolventDichloromethaneHCID 6344—
ProductHCID 86586557HCID 86586557—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Oxalyl chloride (50 mL, 0.10 mmol) was added to CH2Cl2 (150 mL) at 23° C. and was cooled to −78° C. DMSO (16 g, 0.20 mmol) was added dropwise to the mixture and stirring was continued for 15 min. A solution of alcohol 4 (7.9 g, 0.041 mmol) in CH2Cl2 (50 mL) was then added dropwise, after which Et3N (44 g, 0.44 mmol) was added and the mixture was warmed to 23° C. After 1 h, the mixture was poured into saturated aqueous NaHCO3 and the organic layer was separated. The aqueous layer was extracted with CH2Cl2 (2×) and the combined organic portions were washed with brine, dried (Na2SO4), concentrated in vacuo and purified by FCC (silica gel, hexane; 2:1, hexane/CH2Cl2) to afford the above named aldehyde 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376533B1
Source datasetuspto-grants-2002_04
ORD IDord-bee3530dc0df41078961d6cbfb730808
Source noteuspto-grants-2002_04