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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342072Generated: October 30, 2026

Dimethyl Sulfoxide → 2,3-Dihydro-1-benzofuran-4-carbaldehyde

https://huagongshe.com/reaction/342072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(2,3-Dihydro-1-benzofuran-4-yl)methanolHCID 18787415—
SolventDichloromethaneHCID 6344—
Product2,3-Dihydro-1-benzofuran-4-carbaldehydeHCID 18787449—

Reaction Conditions

Temperature-78 °C

Reaction Steps

DMSO (8.10 mL, 114 mmol) was added at -78° C. to a stirred solution of oxalyl chloride in CH2Cl2 (40 mL of a 2M solution). A solution of (2,3-dihydrobenzofuran-4-yl)methanol (8.53 g, 56.9 mmol) in CH2Cl2 (35 mL) was added dropwise, and the solution stirred at -78° C. for 30 min. Triethyl amine (33 mL, 228 mmol) was added cautiously to quench the reaction. The resulting suspension was stirred at room temperature for 30 min and diluted with CH2Cl2 (100 mL). The organic layer was washed three times with water, and twice with brine, and then concentrated in vacuo to an oil (8.42 g, 100%) that was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856529
Source datasetuspto-grants-1999_01
ORD IDord-14cea94e8e704d3fab34d64a8be2efe4
Source noteuspto-grants-1999_01