HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Methyl-4-(oxetan-3-YL)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Methyl-4-(oxetan-3-YL)benzonitrile | HCID 68153309 | — |
| Product | 3-Methyl-4-(oxetan-3-YL)benzoic acid | HCID 68153334 | 14% |
Reaction Steps
To 3-methyl-4-(oxetan-3-yl)benzonitrile (500 mg, 2.89 mmol) in ethanol (7.5 mL) was added NaOH (3.0 mL of 5 M, 15 mmol) and the mixture immersed in a 85° C. oil bath. The mixture was heated and stirred for 1 h, concentrated, then diluted with ethyl acetate (20 mL). 6N HCl (˜3 mL) was added to adjust pH to 6. The aqueous layer was extracted with ethyl acetate (2×20 mL), then the combined organics washed with brine (10 mL), dried over MgSO4 and concentrated to give a white solid, which was triturated with ether to give a mixture (2:3 by NMR) of acid 3-methyl-4-(oxetan-3-yl)benzoic acid (500 mg, 14%) and amide. ESI-MS m/z calc. 192.2, found 193.3 (M+1)+; Retention time: 0.87 minutes (3 min run).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916565B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-14c591baf8314e9982b981f0ceb15712 |
| Source note | uspto-grants-2014_12 |