HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069607Generated: October 29, 2026
Carbon Dioxide → 2-Methyl-1-benzothiophene-7-carboxylic acid
https://huagongshe.com/reaction/2069607
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 7-Bromo-2-methyl-1-benzothiophene | HCID 12623873 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-1-benzothiophene-7-carboxylic acid | HCID 12623903 | 31.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299117B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-ec5f0e6ef3524ddeb5934f2d83b98782 |
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| Source note | uspto-grants-2012_10 |
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