HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methanesulfonyl-6-bromomethylindole → (3-Chloro-4-methyl-5-nitrophenyl) acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methanesulfonyl-6-bromomethylindole | HCID 18789641 | — |
| Reactant | N-methanesulfonyl-6-cyanomethylindole | HCID 18789651 | — |
| Reactant | 5-Bromomethyl-1-chloro-2-methyl-3-nitrobenzene | HCID 18789673 | — |
| Product | (3-Chloro-4-methyl-5-nitrophenyl) acetonitrile | HCID 54125367 | — |
Reaction Steps
(3-Chloro-4-methyl-5-nitrophenyl) acetonitrile was prepared from 5-bromomethyl-1-chloro-2-methyl-3-nitrobenzene in a manner similar to that described in Example 10 for the preparation of N-methanesulfonyl-6-cyanomethyl indole from N-methanesulfonyl-6-bromomethyl indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057349 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-fdab174fc2dc49d79a2f83186a21f4f9 |
| Source note | uspto-grants-2000_05 |