HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Methyl-n-(4-trifluoromethyl-benzyl)-hydroxylamine → 2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-methoxy-n-(4-trifluoromethylbenzyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Methyl-n-(4-trifluoromethyl-benzyl)-hydroxylamine | HCID 23499567 | — |
| Reactant | (2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride | HCID 85435482 | — |
| Product | 2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-methoxy-n-(4-trifluoromethylbenzyl)-acetamide | HCID 73855548 | 97% |
Reaction Steps
Reaction of (2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride with O-methyl-N-(4-trifluoromethyl-benzyl)-hydroxylamine as described in the preparation of compound 1-A gave the title amide as white crystals (97% yield): mp 110° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.76 (6H, s, CH3), 3.71 (3H, s, OCH3), 4.87 (2H, s, NCH2), 6.40 (1H, s, CH), 7.47 (2H, m, aromatics), 7.59 (2H, m, aromatics). Anal. calcd for C16H16F3NO5: C, 53.49; H, 4.49; N, 3.90. Found: C, 53.48; H, 4.53; N, 3.83.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777440B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-73564fc522124135baff78df4458efe1 |
| Source note | uspto-grants-2004_08 |