HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (4S)-4-(3,5-dimethylphenyl)-4-hydroxybutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | ethyl (4S)-4-(3,5-dimethylphenyl)-4-hydroxybutanoate | HCID 86626141 | — |
| Product | (4S)-4-(3,5-dimethylphenyl)-4-hydroxybutanamide | HCID 68997524 | — |
Reaction Steps
A solution of ammonia in methanol (2.0M; 4.02 mL; 8.03 mmol) was treated with ethyl (4S)-4-(3,5-dimethylphenyl)-4-hydroxybutanoate (Step A; 474 mg; 2.01 mmol) and the resultant solution was stirred at 50° C. for 16 h. The reaction was concentrated in vacuo and the residue purified by flash silica gel chromatography (0-100% EtOAc/hexanes gradient) to afford (4S)-4-(3,5-dimethylphenyl)-4-hydroxybutanamide as a white solid. LCMS=190.3 (M+1−18)+. 1H NMR (CDCl3, 500 MHz): δ 7.00 (s, 2H), 6.94 (s, 1H), 5.61 (br s, 1H), 5.40 (br s, 1H), 4.75 (dd, J=7.6, 2.8 Hz, 1H), 2.43-2.39 (m, 2H), 2.34 (s, 6H), 2.12-2.07 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865707B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-3e131b177b3e44ffa4d76bbddbf65a65 |
| Source note | uspto-grants-2014_10 |