HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5297Generated: October 30, 2026
Carbon Dioxide → 3',5-Dimethoxy[1,1'-biphenyl]-2-carboxylic acid
https://huagongshe.com/reaction/5297
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-bromo-5,3'-dimethoxybiphenyl | HCID 11572896 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3',5-Dimethoxy[1,1'-biphenyl]-2-carboxylic acid | HCID 13461694 | — |
Reaction Steps
12.1 g of 6-bromo-3,3'-dimethoxy-biphenyl was dissolved in 100 mL of dry dimethylformamide and the resulting solution was cooled to -60° C. under nitrogen. 55 mL of 1.7 M t-butyllithium in hexanes was added over a 20-minute period. The resulting solution was transferred to another flask containing a mixture of 275 mL of ether and dry ice which effected a lot of gas evolution. The mixture was allowed to warm to room temperature over a 3-hour period during which time a white precipitate had formed. The mixture was diluted with ether and treated with dilute hydrochloric acid and water. The organic layer was separated and the solvents were removed under reduced pressure to yield a yellow oil. Hexanes were added to the oil causing a solid to precipitate out. The solids were filtered and stirred in a 60:40% ether-hexane mixture to remove impurities. The solid was filtered and dried in vacuo to yield 7.82 g of 2-carboxy-5,5'-dimethoxybiphenyl as an off-white solid. The structure was confirmed by NMR and infrared spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244771 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-68533ad2f643465da0032cda5ac4e078 |
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| Source note | uspto-grants-1993_09 |
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