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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909519Generated: November 1, 2026

Carbon Dioxide → 2-Methyl-1-benzothiophene-7-carboxylic acid

https://huagongshe.com/reaction/1909519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant7-Bromo-2-methyl-1-benzothiopheneHCID 12623873—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-1-benzothiophene-7-carboxylic acidHCID 1262390331.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The solution of 7-bromo-2-methylbenzo[b]thiophene (508) (0.908 g, 4.0 mmol) in tetrahydrofuran (16 mL) was cooled to −78° C. under nitrogen. n-butyllithium (2.40 mL, 6.0 mmol, 1.0M in Hexanes) was added dropwise. After the addition was complete, the reaction mixture was stirred at −78° C. for 1 h, then poured on to the mixture of dry ice in ethyl ether (30 mL). The reaction was stirred to reach room temperature for 5 hours, followed by washing with 1N HCl, brine and dried over sodium sulfate, filtered, and concentrated in vacuo. The obtained white solid was washed with hexanes to provide 2-methylbenzo[b]thiophene-7-carboxylic acid (509) (0.240 g, 31.2%). LC-MS ESI m/z: found 191.0 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-f3339f28b72d496fb6a0334c0c657429
Source noteuspto-grants-2013_12