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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant2-bromo-5,3'-dimethoxybiphenylHCID 11572896—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3',5-Dimethoxy[1,1'-biphenyl]-2-carboxylic acidHCID 13461694—

Reaction Conditions

Temperature-60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244771
Source datasetuspto-grants-1993_09
ORD IDord-68533ad2f643465da0032cda5ac4e078
Source noteuspto-grants-1993_09