HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Fluoro-4-methoxy-biphenyl-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Fluoro-4-methoxy-biphenyl-3-carboxylic acid methyl ester | HCID 22093491 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Fluoro-4-methoxy-biphenyl-3-carboxylic acid | HCID 18468199 | 97.1% |
Reaction Steps
To a stirring solution of 6-fluoro-4-methoxy-biphenyl-3-carboxylic acid methyl ester (0.5 g, 2.3 mmol) in dioxane (8 mL, 0.3 M) was added 2N NaOH (6.0 mL, 12 mmol). After one'hour at room temperature, the reaction mixture was concentrated, and 2N HCl was added. The aqueous layer was diluted with ether. The organic layer was separated, dried over Na2SO4, filtered and concentrated to afford a 6-fluoro-4-methoxy-biphenyl-3-carboxylic acid (0.55 g, 96%) as a pale yellow powder: Rf 0.18 (5% methanol in dichloromethane); 1H NMR (CDCl3, 300 MHz) δ 8.35 (d, J=9.0 Hz, 1H), 7.55-7.52 (m, 2H), 7.48-7.38 (m, 3H), 6.89 (d, J=11.7 Hz, 1H), 4.12 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420426B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-d6003dd9e0a94661a2228d60d4c5dee4 |
| Source note | uspto-grants-2002_07 |