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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732964Generated: October 30, 2026

Valeryl chloride → 1-Heptyn-3-one, 1-(trimethylsilyl)-

https://huagongshe.com/reaction/1732964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantValeryl chlorideHCID 61186—
ReactantBis(trimethylsilyl)acetyleneHCID 84564—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-Heptyn-3-one, 1-(trimethylsilyl)-HCID 1101951176%

Reaction Steps

To a stirred solution of 14.4 g of valeryl chloride and 20.4 g of bis-trimethylsilylacetylene in 300 ml of dry methylene chloride, cooled in an ice bath, is added powdered anhydrous aluminum chloride, portionwise, over a period of 20 minutes. The mixture is stirred for 5 minutes, then the cooling bath is removed and the mixture is stirred at room temperature for 4 hours. The mixture is poured into 500 ml of ice-water. The organic layer is separated, washed with water and brine, dried over anhydrous sodium sulfate and filtered through diatomaceous earth. The mother liquor is evaporated to dryness giving a brownish residue. This residue is Kugelrohr-distilled to give 16.56 g of colorless liquid at 45° C./0.3 mm which is essentially identical with the authentic product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239899
Source datasetuspto-grants-1980_12
ORD IDord-b48d730d23f446629ab6295d5a1f34aa
Source noteuspto-grants-1980_12