HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5,6-Tetrahydrophthalic anhydride → 3-Pyridinamine, 6-[(4-chlorophenyl)methoxy]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Product | 3-Pyridinamine, 6-[(4-chlorophenyl)methoxy]- | HCID 580409 | — |
| Product | HCID 20486093 | HCID 20486093 | — |
Reaction Steps
The compound, 5-amino-2-(4-chlorobenzyloxy)pyridine is prepared from 2-chloro-5-nitropyridine and 4-chlorobenzyl alcohol and then reacted with 3,4,5,6-tetrahydrophthalic anhydride using the procedure of Example 1 to yield N-[2-(4-chlorobenzyloxy)-5-pyridyl]-3,4,5,6-tetrahydrophthalimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04406690 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-63ca0f41c7234e3c981b641007fabd40 |
| Source note | uspto-grants-1983_09 |