HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → 5-(4-Bromo-butoxy)-2,3-dimethyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | 2,3-Dimethyl-1H-indol-5-ol | HCID 22030788 | — |
| Product | 5-(4-Bromo-butoxy)-2,3-dimethyl-1H-indole | HCID 18679439 | — |
Reaction Steps
In analogy to example 3.1, 2,3-Dimethyl-1H-indol-5-ol [for preparation see for example: Roth, H. J.; Lepke, P. Synthesis of indole and carbazole derivatives by condensation of α-hydroxyketones and aromatic amines. Arch. Pharm. (Weinheim) (1972), 305(3), 159-71.] and 1,4-dibromobutane were converted to yield 5-(4-Bromo-butoxy)-2,3-dimethyl-1H-indole as white solid, mp 119-120° C., MS: 295 (M, 1Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06503907B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-d5a2774203814af28bdc731b9378eb03 |
| Source note | uspto-grants-2003_01 |