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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464533Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 67823058, compound

https://huagongshe.com/reaction/1464533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium HydroxideHCID 14798—
Reactant(3-Carboxypropyl)(triphenyl)phosphanium bromideHCID 10717451—
Reactant3-(3,5,6-Trimethyl-1,4-dimethoxyphenyl)butanalHCID 19088044—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67823058HCID 6782305868%

Reaction Conditions

Temperature80 °C

Reaction Steps

DMSO (30 ml) was added to sodium hydroxide (1 g, 24 mmole, 60% oil suspension was washed with hexane and dried under reduced pressure) under an atmosphere of argon, followed heating at 80° C. for 1 hour with stirring. After cooling, 3-carboxypropyltriphenyl phosphonium bromide (4.6 g, 11 mmole) was added to the solution, followed by stirring at room temperature. After stirring for 10 minutes, a THF solution (5 ml) of 3-(3,5,6-trimethyl-1,4-dimethoxyphenyl)butanal (2.7 g, 11 mmole) was added dropwise to the mixed solution. The reaction solution was stirred at room temperature for 2 hours, and water (50 ml) was added to it. The organic layer was washed with toluene (100 ml), and the water layer was adjusted to pH 4 with 2N hydrochloric acid, followed by extraction with IPE. The organic layer was washed with water, dried and concentrated under reduced pressure, and the crude product was purified by silica gel column chromatography (eluting solution: IPE) to give 7-(1,4-dimethoxy-3,5,6-trimethylphenyl)-4-octenoic acid (2.2 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304658
Source datasetuspto-grants-1994_04
ORD IDord-a65685501e874bb483112d005e6a9869
Source noteuspto-grants-1994_04