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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606371Generated: October 26, 2026

Triphenylphosphine → 5-Bromo-3-[1-(2-chloro-phenyl)-ethoxy]-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/606371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-(2-Chlorophenyl)ethanolHCID 26082—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantMethyl 5-bromo-3-hydroxythiophene-2-carboxylateHCID 59857018—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-3-[1-(2-chloro-phenyl)-ethoxy]-thiophene-2-carboxylic acid methyl esterHCID 5897049498.2%

Reaction Steps

5-Bromo-3-hydroxy-thiophene-2-carboxylic acid methyl ester (1.67 g, 7/04 mmol, 1.0 Eq.), 1-(2-Chloro-phenyl)-ethanol (1.43 g, 9.16 mmol, 1.3 Eq.) and triphenylphosphine (2.40 g, 9.16 mmol, 1.3 Eq.) were dissolved in anhydrous THF (30 mL) under nitrogen. The resultant solution was cooled to 0° C. and DEAD (1.4 mL, 9.16 mmol, 1.3 Eq.) was added dropwise. The reaction was warmed to ambient temperature and stirred for 4.5 hours. The crude reaction was purified by column chromatography (10% EtOAc/petroleum ether) to give the sub-title compound as a yellow solid (2.60 g, 6.92 mmol, 98%); 1H NMR (400 MHz, CDCl3) δ 1.68 (3H, d), 3.88 (3H, s), 5.71 (1H, q), 6.65 (1H, s), 7.23-7.33 (2H, m), 7.37 (1H, dd), 7.66 (1H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915305B2
Source datasetuspto-grants-2011_03
ORD IDord-ae1a64cb8f9740f3a1ad39dec2f22877
Source noteuspto-grants-2011_03