HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → N-(1-methylcycloheptyl)-2-phthalimidoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-Methylcycloheptan-1-ol | HCID 77376 | — |
| Reactant | N-(Cyanomethyl)-phthalimide | HCID 345881 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(1-methylcycloheptyl)-2-phthalimidoacetamide | HCID 23454147 | — |
Reaction Steps
By processes similar to those described in Examples 1, 2 and 3, phthalimidoacetonitrile (27.9 g.) was caused to react with 1-methylcycloheptan-1-ol (24 g.) in glacial acetic acid solution (90 ml.) at 50° C. by the addition of concentrated sulphuric acid (0 ml.). After the initial vigorous reaction, a further 6 ml. of sulphuric acid wasadded. After 2 hours the resulting N-(1-methylcycloheptyl)-2-phthalimidoacetamide was isolated by pouring into water; it was collected, washed and dried before crystallisation frombenzene; it was obtained as a colourless crystalline solid, m.p. 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277498 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-3ac0f61878a14e4bb2e06187a018c908 |
| Source note | uspto-grants-1981_07 |