HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Pentanol → Phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Pentanol | HCID 6276 | — |
| Reactant | 4-(Aminosulfonyl)-5-chlorophthalimide | HCID 19733 | — |
| Reactant | 4-Amino-1-[4-(2-propenyloxy)benzyl]piperidine | HCID 23312445 | — |
| Product | Phthalimide | HCID 6809 | — |
Reaction Steps
Reaction of 4-chloro-5-sulfamoylphthalimide (4.54 g., 0.0174 mole) and 4-amino-1-[4-(2-propenyloxy)benzyl]piperidine (4.29 g., 0.0174 mole) in 100 ml. of n-pentanol at reflux temperature for 24 hrs. according to the procedure of Example 1(a) afforded crude 1,3-dioxoisoindole product. Purification was carried out by treating with methanol-decolorizing charcoal followed by trituration with ether to afford 4.8 g. (57%) of the 1,3-dioxoisoindole used without further purification below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04495194 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-4e92a7ed10eb4433a93ae225d95661fb |
| Source note | uspto-grants-1985_01 |