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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552276Generated: October 26, 2026

Methyl iodide → 5-Ethyl-4-phenyl-thiophene-2-carboxylic acid

https://huagongshe.com/reaction/552276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-Phenylthiophene-2-carboxylic acidHCID 1223184—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-Ethyl-4-phenyl-thiophene-2-carboxylic acidHCID 67166421—

Reaction Steps

At −78° C., a solution of 4-phenylthiophene-2-carboxylic acid (800 mg, 3.92 mmol) in THF (10 mL) is treated with tert.-BuLi (8 mL, 1.6 M in pentane). The mixture is stirred at −70° C. for 40 min before iodomethane (1 mL) is added. Stirring is continued for 5 h at −78° C., then the reaction mixture is allowed to warm to rt overnight. The reaction is quenched with sat. aq. NH4Cl and extracted with EA. The organic extract is dried over MgSO4, the solvent is removed and the crude product is purified by CC on silica gel eluting with DCM containing 3% of methanol to give 5-ethyl-4-phenyl-thiophene-2-carboxylic acid (340 mg) as a red solid; LC-MS: tR=0.95 min, [M+1+MeCN]+=274.15; 1H NMR (CDCl3): δ 7.79 (s, 1H), 7.46-7.31 (m, 5), 2.92 (q, J=7.6 Hz, 2H), 1.30 (t, J=7.6 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951794B2
Source datasetuspto-grants-2011_05
ORD IDord-de21b785213f4e0dab0ab4e16f655673
Source noteuspto-grants-2011_05