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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094290Generated: November 1, 2026

1-Bromo-2-methylpropane → 5-(2-Methylpropyl)thiophene-2-carboxylic acid

https://huagongshe.com/reaction/1094290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Thiophenecarboxylic acidHCID 10700—
Product5-(2-Methylpropyl)thiophene-2-carboxylic acidHCID 1962268928.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-thiophene-carboxylic acid (4.16 g, 32.1 mmol) in THF (200 mL) tert. butyllithium (49 mL, 1.7 M solution in pentane, 83.6 mmol) is slowly added at −78° C. The mixture is stirred at −78° C. for 30 min before isobutylbromide (22.7 g, 160.7 mmol) is carefully added. The mixture is stirred at −78° C. for 5 h, then at rt for 16 h. The reaction is quenched by the addition of water (400 mL). The mixture is acidified and extracted with EA. The org. extract is dried over MgSO4, filtered and evaporated. The crude product is purified by MPLC on reverse phase silica gel to give the title compound (1.67 g) as a brownish oil; LC-MS: tR=0.91 min, 1H NMR (CDCl3): δ 0.96 (d, J=6.7 Hz, 6H), 1.94 (hept, J=6.7 Hz, 1H), 2.72 (d, J=7.0 Hz, 2H), 6.80 (d, J=3.8 Hz, 1H), 7.73 (d, J=3.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133910B2
Source datasetuspto-grants-2012_03
ORD IDord-5cd44082c49845b890aa93d09c82fe13
Source noteuspto-grants-2012_03