HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098934Generated: November 1, 2026
Dimethylformamide → [1,1′-Biphenyl]-4-carboxylic acid, 2-(6,6-dimethyl-1-cyclohexen-1-yl)-2′-fluoro-5′-methoxy-, methyl ester
https://huagongshe.com/reaction/2098934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57467612 | HCID 57467612 | — |
| Reactant | Methyl 2'-fluoro-2-iodo-5'-(methyloxy)-1,1'-biphenyl-4-carboxylate | HCID 57705628 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | [1,1′-Biphenyl]-4-carboxylic acid, 2-(6,6-dimethyl-1-cyclohexen-1-yl)-2′-fluoro-5′-methoxy-, methyl ester | HCID 57706936 | 48.6% |
Reaction Steps
To a stirred solution of T10.4 (0.750 g, 1.9 mmol) in DMF (4.00 mL, 52 mmol) at 23° C. was added T14.2 (0.92 g, 3.9 mmol), potassium carbonate (0.81 g, 5.8 mmol), and then tetrakis(triphenylphosphine)palladium (0.22 g, 0.19 mmol). The mixture was heated to 90° C. and stirred for 24 hours. The reaction was then cooled to room temperature, diluted with brine, and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was then purified on silica gel (0-10% EtOAc in hexanes) to yield T14.3 as a colorless oil (0.34 g, 48% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08450522B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-dfc32980da93495ea9df5d5123475912 |
|---|
| Source note | uspto-grants-2013_05 |
|---|