Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915642Generated: October 31, 2026

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

https://huagongshe.com/reaction/915642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium HydroxideHCID 14798—
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 Conditions

Temperature-78 °C

Reaction Steps

Dissolve crude 3,5-difluorobiphenyl (1.3 g, 6.83 mmol) in tetrahydrofuran (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 tetrahydrofuran (14 mL). Cannulate the cooled LiTMP into the cooled 3,5-difluorobiphenyl and stir the reaction at −78° C. for 1 hour. Bubble carbon dioxide gas through the solution for 5 minutes, warm the reaction to room temperature, pour into 50 mL of 1M sodium hydroxide, and extract with 50 mL ethyl acetate. Discard the organic layer. Acidify the remaining aqueous layer with conc. HCl and extract twice with ethyl acetate. Dry the organics over magnesium sulfate, 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 numberUS07265246B2
Source datasetuspto-grants-2007_09
ORD IDord-b5d93b37e60b4eea83e73aaaf9864d9c
Source noteuspto-grants-2007_09