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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700930Generated: October 31, 2026

Triphenylphosphine → HCID 22949960, compound

https://huagongshe.com/reaction/1700930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantEthanol, 2-(dodecylthio)-HCID 73835—
ReactantBenzenepropanoic acid, 4-hydroxy-, methyl esterHCID 79706—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 22949960HCID 2294996084.6%

Reaction Steps

A solution of methyl 3-[4-hydroxyphenyl)propionate (2.46 g, 13.6 mmol), 2-(dodecylthio)ethanol (3.40 g, 13.7 mmol) and triphenylphosphine (3.60 g, 13.8 mmol) in dry benzene (50 ml) was treated at 22° C. with diethyl azodicarboxylate (2.43 g, 13.9 mmol) added dropwise over 10 min. After 3 h at 22° C., the reaction mixture was diluted with ethyl acetate, washed with water, brine and dried (magnesium sulfate). Evaporation under reduced pressure gave an oil which was triturated with hexane to precipitate the triphenylphosphine oxide and the hydrazine side products. The filtrate was chromatographed on silica gel using a gradient of ethyl acetate (0-5%) in hexane as eluent to give 4.70 g(84%) of 3-[4-[2-(dodecylthio)ethoxy]phenyl]propanoic acid methyl ester as a white solid. Recrystallization from methanol gives white leaflets: m.p. 48° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-e4d046258b4b46298f8cb405907f75f7
Source noteuspto-grants-2002_02