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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395616Generated: October 31, 2026

Acetylene → HCID 13434207, compound

https://huagongshe.com/reaction/1395616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantOctanoyl chlorideHCID 8124—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 13434207HCID 13434207—

Reaction Steps

A solution of 200 ml of octanoyl chloride (A6, R1 =C2H5) in 750 ml of carbon tetrachloride is cooled on an ice bath and treated with 214 g of aluminium chloride in three portions over a 1 hour period while acetylene is bubbled through the solution. The ice bath is removed and the reaction mixture stirred at room temperature for 3 hours with additional acetylene being added. At the end of this period, the reaction mixture is poured into 4 kg of ice. The organic layer is separated and the aqueous layer extracted twice with 500 ml of chloroform. The combined organic extracts are washed once with 500 ml of water, dried over anhydrous sodium sulfate and concentrated in vacuo. Distillation of the residue yields 142 g of trans-1-chloro-dec-1-en-3-one, (A5, R1 =C2H5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030287
Source datasetuspto-grants-1980_05
ORD IDord-4aec0d18417c4740a6a3d867285e6d8f
Source noteuspto-grants-1980_05