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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053698Generated: October 30, 2026

Carbon Dioxide → 3,5-Difluorobiphenyl-4-carboxylic acid

https://huagongshe.com/reaction/2053698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant3,5-DifluorobiphenylHCID 13022391—
Reactant1,2,2,3-TetramethylpiperidineHCID 18761772—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418821HCID 178418821—
SolventTetrahydrofuranHCID 8028—
Product3,5-Difluorobiphenyl-4-carboxylic acidHCID 4631476877%

Reaction Steps

Dissolve crude 3,5-difluorbiphenyl (1.3 g, 6.83 mmol) in THF (14 mL) and cool to. −78° C. Prepare LiTMP from the addition of BuLi (1.6 M soln in hexanes, 5.33 mL) to tetramethyl piperidine (1.4 mL, 1.25 equiv) at −78° C. in THF (14 mL). Cannulate the cooled LiTMP into the cooled 3,5-difluorobiphenyl and stir the reaction at −78° C. for 1 h. Bubble carbon dioxide gas through the solution for 5 minutes, warm the reaction to rt, pour into 50 mL of 1M NaOB, and extract with 50 mL EtOAc. Discard the organic layer was discarded. Acidify the remaining aqueous layer with conc. HCl and extract twice with EtOAc. Dry the organics over MgSO4, filtered, and evaporate to give 1.22 g of the title compound as a white solid (77%). MS (m/e): 233.1 (M−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326731B2
Source datasetuspto-grants-2008_02
ORD IDord-91a66127e69f454ebb20ae79a1a0f2f3
Source noteuspto-grants-2008_02