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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413564Generated: October 30, 2026

Dimethyl Sulfoxide → (+/-)-7-(4-Fluorophenoxy)-6-(2-methoxyethoxymethoxy)-heptan-1-al

https://huagongshe.com/reaction/413564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant(+/-)-7-(4-Fluorophenoxy)-6-(2-methoxyethoxymethoxy)heptan-1-olHCID 18533434—
SolventDichloromethaneHCID 6344—
Product(+/-)-7-(4-Fluorophenoxy)-6-(2-methoxyethoxymethoxy)-heptan-1-alHCID 18533431—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Oxalyl chloride (2.9 ml, 33.6 mmol) is added to 25 ml of methylene chloride and cooled to −78° C. Dry dimethyl sulfoxide (4.7 ml, 67.2 mmol) is then added and the reaction is stirred at −78° C. After 45 minutes, (±)-7-(4-fluorophenoxy)-6-(2-methoxyethoxymethoxy)-heptan-1-ol 44 (3.7 g, 11.2 mmol) dissolved in CH2Cl2 is added and the reaction is stirred at −78° C. After 1 hour, the reaction is quenched with 15.7 ml of triethylamine and diluted with CH2Cl2. The reaction mixture is then washed with water, brine dried (Na2SO4) and concentrated. The crude product is purified on silica gel (ethyl acetate:hexane 1:9) to give (±)-7-(4-fluorophenoxy)-6-(2-methoxyethoxymethoxy)-heptan-1-al 45, 3.3 g, 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566538B1
Source datasetuspto-grants-2003_05
ORD IDord-344ae656ea1c4a179374800e162cde16
Source noteuspto-grants-2003_05