HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2-iodobenzene → 1-(2-Chlorophenyl)-3-(2-hydroxyiminopropyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2-iodobenzene | HCID 11993 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(2-Chlorophenyl)-3-(2-oxopropyl)indole | HCID 21543502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Chlorophenyl)-3-(2-hydroxyiminopropyl)indole | HCID 53936023 | 71% |
Reaction Steps
2.1 G (0.03 mole) of hydroxylamine hydrochloride and 2.1 g of sodium acetate are added, all at once, to 5.8 g (0.02 mole) of 1-(2-chlorophenyl)-3-(2-oxopropyl)indole prepared as described in example 1 but using 2-chloroiodobenzene instead of iodobenzene are dissolved in 50 ml of ethanol. The mixture is stirred overnight. The oxime formed is then filtered, washed in water and recrystallised, after drying, from 30 ml of di-isopropyl ether. Product = 4.3 g: Melting point (k) = 127°. Yield = 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933853 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-29a0b1b2d1cf4bf7ad950c7ba4e78e3c |
| Source note | uspto-grants-1976_01 |