Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284461Generated: November 1, 2026

Water → HCID 13417266, compound

https://huagongshe.com/reaction/1284461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenyl-3-pyridinylmethanoneHCID 21540—
ReactantSodium hydrideHCID 24758—
ReactantPhosphonium, (10-carboxydecyl)triphenyl-, bromideHCID 11432504—
SolventDimethyl SulfoxideHCID 679—
SolventHexaneHCID 8058—
ProductHCID 13417266HCID 1341726626.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

Sodium hydride (60% dispersion in oil, 2.7 g, 68 mmoles) was washed with hexane and, after removal of the hexane under reduced pressure, dimethyl sulfoxide (40 ml) was added and the mixture was stirred with heating at 85° C. for an hour. After cooling, a dimethyl sulfoxide solution (20 ml) containing 10-carboxydecyltriphenylphosphonium bromide (18.0 g, 34 mmoles) was added dropwise to the mixture. After 10 minutes, a solution of 3-benzoylpyridine (6.2 g, 33.8 mmoles) in dimethyl sulfoxide (10 ml) was added. The reaction was allowed to proceed for an hour and, following addition of water (200 ml), the reaction product was washed with toluene. The aqueous layer was acidified with 2N hydrochloric acid to pH 5.2, and the product was extracted with ethyl acetate. The organic layer was washed with water, dried and distilled under reduced pressure to remove the solvent. The residue was then subjected to silica gel column chromatography using ethyl acetate as the developing solvent to give (Z)-12-phenyl-12 -(3-pyridyl)-11-dodecenoic acid (Compound Id-8, 3.2 g), after fractional recrystallization from isopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563446
Source datasetuspto-grants-1986_01
ORD IDord-443bd2d8607543198f2d7ad6bc89eb33
Source noteuspto-grants-1986_01