HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride, 3-nitro- → HCID 18506156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | HCID 18506136 | HCID 18506136 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18506156 | HCID 18506156 | — |
Reaction Steps
2-[3,4-Bis-(1-benzyl-1H-tetrazol-5-yl)phenoxy]phenylamine (37 mg, 0.07 mmol) and TEA (19 mg, 0.18 mmol) were mixed in acetone (10 ml), and 3-nitrobenzoyl chloride (15 mg, 0.08 mmol) was added. The reaction mixture was stirred for 120 hours at room temperature. The reaction mixture was evaporated in vacuo to an oil. The oil was purified on a silica column with methylene chloride/methanol (39:1) as eluent. The title compound was isolated as yellow oil (yield: 30 mg (62%). 1H-NMR (CDCl3 in ppm): 5.6 (4H,2xs); 7.0 (1H,d,d); 7.15 (1H,d,d); 7.2 (1H,d,d); 7.25-7.4 (11H,m); 7.6 (1H,d,d); 7.73 (1H,d); 7.9 (1H,d); 8.1 (1H,d,d); 8.35 (1H,d,d); 8.45 (1H,broad s); 8.55 (1H,d,d); 8.7 (1H,d,d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06590118B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-0027b81ff3764a21913fd50c5502472c |
| Source note | uspto-grants-2003_07 |