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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268259Generated: November 1, 2026

Tributylphosphine → (E)-(S)-ethyl 3-{4-[3-(4-bromophenyl)-but-2-enyloxy]-phenyl}-2-ethoxy-propionate

https://huagongshe.com/reaction/1268259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantEthyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 9816147—
Reactant(E)-3-(4-bromophenyl)but-2-en-1-olHCID 69361278—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(E)-(S)-ethyl 3-{4-[3-(4-bromophenyl)-but-2-enyloxy]-phenyl}-2-ethoxy-propionateHCID 86589946—

Reaction Steps

Azodicarboxylic dipiperidide (0.756 g, 3.0 mmol) was added at 0-5°C. to a stirred solution of tributylphosphine (0.74 ml, 0.61 g, 3.0 mmol), (S)-ethyl 2-ethoxy-3-(4-hydroxyphenyl)-propionate (0.500 g, 2.10 mmol) and (E)-3-(4-bromophenyl)-but-2-en-1-ol (0.454 g, 2.0 mmol) in dry benzene (20 ml), the mixture warmed to room temperature, and stirred for 2.5 days. The resulting mixture was diluted with water and ethyl acetate (50 ml each), the aqueous layer collected and further extracted with ethyl acetate (50 ml). The organic layers were combined, washed with brine, dried (MgSO4) and evaporated. The crude product was then purified by column chromatography on silica gel (20% ethyl acetate in n-heptane eluent) to give (E)-(S)-ethyl 3-{4-[3-(4-bromophenyl)-but-2-enyloxy]-phenyl}-2-ethoxy-propionate as an oil; 0.780 g (87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555577B1
Source datasetuspto-grants-2003_04
ORD IDord-cb91614824dc4177afe870a5e7cfa93b
Source noteuspto-grants-2003_04