HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879141Generated: October 30, 2026
2,6-Difluorophenylboronic acid → HCID 66652899, compound
https://huagongshe.com/reaction/879141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Difluorophenylboronic acid | HCID 2734336 | — |
| Reactant | 2-Chloropyrimidine-4-carboxylic acid | HCID 22135751 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 66652899 | HCID 66652899 | — |
Reaction Steps
To a solution of 2-chloropyrimidine-4-carboxylic acid (1.0 equiv.) in DME and 2M Na2CO3 (3:1, 0.25 M) was added 2,6-difluorophenylboronic acid (1.3 equiv.) and Pd(dppf)Cl2-DCM (0.05 equiv.) in a microwave vial. The vial was heated in the microwave at 120° C. for 30 minutes. The mixture was diluted with ethyl acetate and 1N NaOH was added. The organic phase was separated and extracted three more times with 1N NaOH and once with 6N NaOH. The combined aqueous phases were filtered and acidified to pH 1 by the addition of concentrated HCl and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated to give 2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid in 81%. LCMS (m/z): 237.0 (MH+), Rt=0.54 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987457B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-dd321826814d4aa4b20b3bd6cbf0b5eb |
|---|
| Source note | uspto-grants-2015_03 |
|---|