HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 9925962, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 21997646 | HCID 21997646 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9925962 | HCID 9925962 | — |
Reaction Steps
The title compound was prepared by base catalyzed ring closure of N-(2-cyanomethylsulfonyl-5-trifluoromethylphenyl)-acetamide by a procedure analogous to the procedure described in EXAMPLE 1 c); white flakes (from methanol), mp 329-333° C., 1H-NMR(CD3OD) δ (ppm): 8.20-8.10 (br d, 1H), 7.78-7.62 (m, 2H), 4.88 (br, H2O+NH), 2.52 (s, 3H); 13C-NMR (DMSO-d6) δ (ppm): 156.4, 135.6, 133.1 (q, J=33 Hz), 126.6, 124.2, 123.0 (CF3, J=273 Hz), 121.9 (J=3.4 Hz), 116.2 (J=4.5 Hz), 112.4 (C≡N), 86.3 20.4; IR (KBr) ν (cm−1): 3301, 3195, 3133, 2214(C≡N), 1628, 1614, 1592, 1554, 1487, 1422, 1339, 1308, 1265, 1241, 1187, 1159, 1131, 1083, 890; MS m/e (rel. intensity): 288 (74%, M+), 224 (74%), 223 (100%), 203 (8%), 155 (9%), 69 (16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232310B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-b3ade8d49b7b4ef59235ce5b61ad4755 |
| Source note | uspto-grants-2001_05 |