HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 1-(5-Chloropentyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Reactant | 1-(6-Chlorohexyl)-1H-indole | HCID 12340759 | — |
| Product | 1-(5-Chloropentyl)-1H-indole | HCID 12340758 | 80% |
Reaction Steps
According to the procedure used for the synthesis of 1-(6-chlorohexyl)-1H-indole, 1-H-indole (0.585 g, 5.00 mmol) and 1-bromo-5-chloropentane (0.928 g, 5.00 mmol) gave the desired product (0.890 g, 80%). 1H NMR (CDCl3) δ 7.76-7.51 (m, 1H), 7.44-6.96 (m, 4H), 6.60-6.38 (m, 1H), 4.11 (t, 2H, J=6.8 Hz), 3.47 (t, 2H, J=6.4 Hz), 1.97-1.79 (m, 2H), 1.79-1.61 (m, 2H), 1.58-1.32 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06727264B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-ac507f40740f496e887420f12c3d8ae7 |
| Source note | uspto-grants-2004_04 |