HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylethylamine → 1-(3,4-dichlorophenyl)-N-ethyl-N-methylcyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | HCID 594622 | HCID 594622 | — |
| Product | 1-(3,4-dichlorophenyl)-N-ethyl-N-methylcyclohexanecarboxamide | HCID 68674635 | 30% |
Reaction Steps
The amide was synthesized from 1-(3,4-dichlorophenyl)-cyclohexanecarboxylic acid (390 mg, 1.43 mmol) and ethylmethylamine using General Procedure G and was isolated in 30% yield as a white solid. HPLC Rt=11.66 min; 1H NMR (400 mHz, CDCl3) 7.40-7.30 (m, 2H), 7.10 (dd, J=2.2, 8.4 Hz, 1H), 3.31 (bs, 2H), 2.59 (bs, 3H), 2.30 (d, J=12.5 Hz, 2H), 1.76-1.55 (m, 7H), 1.32-1.25 (m, 2H), 1.00 (bs, 3H); 13C NMR (100 mHz, CDCl3) 147.0, 132.9, 130.8, 130.3, 127.5, 125.2, 51.0, 44.5, 36.8, 25.9, 23.5; GC-MS (SCOUT) 13.01 min, M+ 313.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877975B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-3229ed333e924b6597d2040e8a03e93b |
| Source note | uspto-grants-2014_11 |