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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303683Generated: November 1, 2026

Dimethyl Sulfoxide → (+)-trans-3-Formyl-4-phenylcyclopentan-1-one

https://huagongshe.com/reaction/2303683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant(+)-trans-3-Hydroxymethyl-4-phenylcyclopentan-1-oneHCID 53754795—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(+)-trans-3-Formyl-4-phenylcyclopentan-1-oneHCID 54453591—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of oxalyl chloride (0.352 mL, 0.512 g, 4.03 mmol) in methylene chloride (8 mL) at −70° C. was added dropwise DMSO (0.573 mL, 0.630 g, 8.06 mmol). After 10 min, a solution of (+)-trans-3-hydroxymethyl-4-phenylcyclopentan-1-one from Example 11, Step F (0.153 g, 0.807 mmol) in methylene chloride (1 mL) was added dropwise. The reaction mixture was stirred at −70° C. for 45 min and then diisopropylethylamine (2.1 mL, 1.6 g, 4.48 mmol) was added. The reaction mixture was allowed to warm to rt for 10 min and then diluted with methylene chloride, poured into water, and extracted three times with methylene chloride. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude title compound (0.15 g) was used directly in Step B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-81240fd29b0644689b861ae0c90fcb60
Source noteuspto-grants-2002_08