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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917955Generated: October 26, 2026

Acetylene → 1-Chloro-6-phthalimidohex-1-en-3-one

https://huagongshe.com/reaction/917955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
Reactant4-(1,3-Dioxoisoindolin-2-yl)butanoyl chlorideHCID 594886—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1,2,2-TetrachloroethaneHCID 6591—
Product1-Chloro-6-phthalimidohex-1-en-3-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03968216
Source datasetuspto-grants-1976_07
ORD IDord-4080ad020c2844d3aae0d54dfe32d5fc
Source noteuspto-grants-1976_07