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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566836Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 21263620, compound

https://huagongshe.com/reaction/566836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21263622HCID 21263622—
SolventDichloromethaneHCID 6344—
ProductHCID 21263620HCID 2126362077.4%

Reaction Conditions

Temperature-45 °C

Reaction Steps

A solution of oxalyl chloride (42 mL) in dry methylene dichloride (750 mL) was cooled under a nitrogen atmosphere to −75° C. Dimethylsulfoxide (72 mL) was added dropwise with stirring, followed after 10 minutes by a solution of 4-(n-heptyloxy)butan-1-ol (75.2 g from below) in methylene dichloride (75 mL). The mixture was stirred and allowed to warm to −45° C., then was again cooled to −75° C. and treated dropwise with triethylamine (292 mL). After the addition was complete, the cooling bath was removed and the mixture was allowed to slowly warm to room temperature and stir one hour. Ice was added, and the product was partitioned between water and methylene dichloride. The solvent was removed with a rotary evaporator, and the residue was dissolved in petroleum ether (500 mL) and the solution was rinsed in water, cold aqueous hydrochloric acid, water, and saturated aqueous sodium bicarbonate. After drying over magnesium sulfate, the solvent was stripped in vacuo, and the residue was distilled to give 57.6 g (77%) of 4-(n-heptyloxy)butanal, b.p. 60° C., 0.26 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177073B1
Source datasetuspto-grants-2001_01
ORD IDord-3776a3bf675c4d388a314fc187c4eb43
Source noteuspto-grants-2001_01