HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-[(Pyridin-2-yl)sulfanyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 23023086 | HCID 23023086 | — |
| Reactant | HCID 23023091 | HCID 23023091 | — |
| Product | 4-[(Pyridin-2-yl)sulfanyl]aniline | HCID 18971660 | — |
Reaction Steps
4-(3-Thienylthio)aniline: 4-(3-Thienylthio)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method B1. A13j. General Method for Substituted Aniline Formation via Nitroarene Formation Through Nucleophilic Aromatic Substitution, Followed by Reduction
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517880B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-12c12cd7470f49bfa76d672f31b36d66 |
| Source note | uspto-grants-2009_04 |