HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylene → 1-Chloro-6-phthalimidohex-1-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | 4-(1,3-Dioxoisoindolin-2-yl)butanoyl chloride | HCID 594886 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| Product | 1-Chloro-6-phthalimidohex-1-en-3-one | HCID 53737306 | — |
Reaction Steps
Aluminum chloride (43 g) is added to a stirred solution of 4-phthalimidobutyryl chloride (36.2 g) in 1,1,2,2-tetrachloroethane (400 ml), previously saturated with acetylene. Acetylene is bubbled through the solution overnight, with stirring, and the reaction mixture is then decomposed by the addition of crushed ice (300 g). The organic layer is separated and the aqueous layer extracted with 1,1,2,2-tetrachloroethane (3 × 100 ml). The combined organic solution is dried over sodium sulphate and concentrated. The residual solid is recrystallized from hexane affording 1-chloro-6-phthalimidohex-1-en-3-one, m.p. 92°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03968216 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-4080ad020c2844d3aae0d54dfe32d5fc |
| Source note | uspto-grants-1976_07 |