HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289433Generated: October 26, 2026
Carbon Dioxide → 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan-2-carboxylic acid
https://huagongshe.com/reaction/2289433
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan | HCID 54518756 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-n-Butylidene-4,5,6,7-tetrahydrobenzo[b]furan-2-carboxylic acid | HCID 54005621 | — |
Reaction Steps
To a mixture of 1.66 N n-butyl lithium (nBuLi) (328 m in n-hexane solution) and Et2O (100 ml) was added a mixture of 4-n-butylidene-4,5,6,7-tetrahydrobenzo[b]furan (9.60 g) and Et2O (50 ml) dropwise over 5 minutes while maintaining -30~-20° C. by dry ice--carbon tetrachloride (CCl4) cooling. The reaction mixture was stirred at r.t. for 1 hour, and was bubbled by carbon dioxide (CO2) gas for 1 hour. The whole mixture was stirred at r.t. overnight and poured into a mixture of water and Et2O. The separated aqueous layer was adjusted to pH 1.4 with 10% HCl, and extracted by AcOEt. The organic layer was washed with brine, dried over MgSO4, and evaporated to give 4-n-butylidene-4,5,6,7-tetrahydrobenzo[b]-furan-2-carboxylic acid (3.91 g) as a reddish oil, which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093710 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-9a30b421d6bc4437990d8b09019244d3 |
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| Source note | uspto-grants-2000_07 |
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