HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → HCID 22237598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 4-(Chlorosulfonyl)-2-hydroxybenzoic acid | HCID 14668531 | — |
| Reactant | HCID 22237385 | HCID 22237385 | — |
| Product | HCID 22237598 | HCID 22237598 | — |
Reaction Steps
The title compound was prepared as a white solid (0.388 g, 40%) from 3-bromo-4-hydroxy-N-(8-phenyloctyl)benzamide and 4-chlorosulfonyl-2-hydroxy-benzoic acid using a procedure similar to step 3 of Example 179. 1H NMR (DMSO-d6) δ8.57 (bt, 1H); 8.50 (d, 1H); 7.99 (dd, 1H); 7.86 (dd, 1H); 7.38-7.32 (m, 3H); 7.26-7.10 (m, 5H); 3.50 (bs, 2H); 3.20 (dd, 2H); 2.53 (t, 2H); 1.50 (m, 4H); 1.28 (m, 8H); IR (KBr) 3480, 3350, 2950, 2850, 1900, 1690, 1630, 1600, 1580, 1540, 1480, 1450, 1360, 1285, 1250, 1205, 1180, 1110, 1080, 1040, 930, 860 cm−1; mass spectrum [(+)APCI], r/z 604 (M+H)+; Anal. Calcd. for C28H30BrNO7S: C, 55.63; H, 5.00; N, 2.32, Found: C, 54.33; H, 5.11; N, 1.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214877B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-705fc5a20b404f15b799d61169cf21b1 |
| Source note | uspto-grants-2001_04 |