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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439678Generated: October 25, 2026

Acetylene → 1-Bromo-trans-1-octen-3-one

https://huagongshe.com/reaction/1439678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
Reactant1,2-DibromoethaneHCID 7839—
ReactantBromhydrolHCID 166749—
ReactantHexanoyl bromideHCID 13226800—
SolventSodium chloride; waterHCID 57417360—
Product1-Bromo-trans-1-octen-3-oneHCID 11790338—

Reaction Steps

A mixture of 300 g. of aluminum bromide and 250 ml. of 1,2-dibromoethane, cooled in an ice bath and protected from moisture, is saturated with acetylene. To the mixture is added with ice cooling 150 g. of hexanoyl bromide (Example 991) over a period of 20 minutes and the resulting mixture is treated with acetylene until gas uptake ceases. The reaction mixture is poured onto 500 ml. of saturated brine and 500 g. of ice. The resulting mixture is extracted twice with 500 ml. of ether. The combined organic extracts are washed twice with 500 ml. of saturated brine and dried with anhydrous sodium sulfate. To the organic phase is added 5 g. of hydroquinone and the solvent is evaporated in vacuo to yield the crude 1-bromo-trans-1-octen-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04060540
Source datasetuspto-grants-1977_11
ORD IDord-ead971837514437ea0a40b374546879b
Source noteuspto-grants-1977_11