HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(7-chloro-6-oxooctyl)phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diazoethane | HCID 70695 | — |
| Reactant | N-(6-Chloro-6-oxohexyl)phthalimide | HCID 594868 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(7-chloro-6-oxooctyl)phthalimide | HCID 23330871 | — |
Reaction Steps
A solution of 6-phthalimidohexanoyl chloride (2 g.) in dry toluene was added to an ethereal solution of diazoethane at -78° C. and the mixture was allowed to warm to room temperature and stand for 15 hours. On standing a solid crystallized out of solution. The reaction mixture was filtered and the filtrate evaporated to dryness giving 1.43 g. of yellow-green oil. This oil was then dissolved in acetone and concentrated hydrochloric acid added until effervescence ceased. The resulting yellow-brown solution was then evaporated to dryness and azeotroped three times with toluene to give N-(7-chloro-6-oxooctyl)phthalimide (1.4 g.) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04165377 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-a29164592f604bc480bf82c469987066 |
| Source note | uspto-grants-1979_08 |