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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188232Generated: November 1, 2026

Hydrochloric Acid → HCID 66874934, compound

https://huagongshe.com/reaction/1188232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant2,6-DimethylbenzaldehydeHCID 583841—
ReactantPhosphonium, (8-carboxyoctyl)triphenyl-, bromideHCID 10918084—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66874934HCID 66874934—

Reaction Steps

Sodium hydride (60% dispersion in mineral oil; 0.65 g, 16 mmol) was added portionwise at room temperature to a stirred solution of (8-carboxy-octyl)-triphenyl-phosphonium bromide (2.8 g, 5.6 mmol) in tetrahydrofuran (30 mL) at room temperature, then after 1 hour 2,6-dimethylbenzaldehyde (757 mg, 5.64 mmol) was added portionwise to the reaction mixture and the solution stirred for 2 days at room temperature. On reaction completion, water (10 ml) was added and the solution acidified to pH 3 with concentrated hydrochloric acid. The product was extracted with ethyl acetate, the organic layer dried over magnesium sulfate, filtered and evaporated. Chromatography (SiO2, heptane-ethyl acetate 4:1) afforded 10-(2,6-dimethyl-phenyl)-dec-9-enoic acid as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673946B2
Source datasetuspto-grants-2014_03
ORD IDord-42b9291f777743158546181e05f299f5
Source noteuspto-grants-2014_03