HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 2'-Cyano-5-(hydroxymethyl)-4'-methylbiphenyl-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2'-cyano-5-(hydroxymethyl)-4'-methylbiphenyl-3-carboxylate | HCID 58187956 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'-Cyano-5-(hydroxymethyl)-4'-methylbiphenyl-3-carboxylic acid | HCID 58188342 | — |
Reaction Steps
To a stirred solution of methyl 2′-cyano-5-(hydroxymethyl)-4′-methylbiphenyl-3-carboxylate (220 mg, 0.78 mmol) in 1,4-dioxane (5 mL) and water (1 mL) was added lithium hydroxide (60 mg, 2.5 mmol). The reaction mixture was stirred at rt for 8 h, and then treated with aq. NH4Cl and EtOAc. The organic layer was separated, dried over anhydrous MgSO4, and concentrated. The residue was purified by silica gel chromatography to afford the title compound. 1H NMR (acetone-d6, 400 MHz): 8.16 (m, 1H), 8.11 (m, 1H), 7.81 (m, 1H), 7.73 (m, 1H), 7.65-7.61 (m, 1H), 7.56 (d, 1H, J=8.0 Hz), 4.81 (s, 2H), 2.46 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946439B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-05c5e1b0124749b193f10313bf558961 |
| Source note | uspto-grants-2015_02 |