HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropylamine → HCID 12953788, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 1-Phenyl-2,3-naphthalenedicarboxylic anhydride | HCID 226666 | — |
| Product | HCID 12953788 | HCID 12953788 | — |
Reaction Steps
1-Phenyl-2,3-naphthalenedicarboxylic anhydride (3.0 g) and cyclopropylamine (5 ml) were shaken for 5 minutes. The reaction mixture became very warm and excess cyclopropylamine was evaporated in vacuo. The solid remaining was then heated at 220° to 240° for 5 minutes in a nitrogen atmosphere. The solid formed was allowed to cool and was recrystallised from light petroleum (b.p. 40°-60°)/chloroform to give 2-cyclopropyl-1,3-dioxo-4-phenylbenz[f]isoindoline, (2.7 g, m.p. 198°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351842 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-4e43e1781c984964b9b4263ee5f94e77 |
| Source note | uspto-grants-1982_09 |