HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126723Generated: October 26, 2026
Valeryl chloride → 1-Heptyn-3-one, 1-(trimethylsilyl)-
https://huagongshe.com/reaction/126723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | Bis(trimethylsilyl)acetylene | HCID 84564 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Heptyn-3-one, 1-(trimethylsilyl)- | HCID 11019511 | — |
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 l 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254036 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-7a3e0c249c8d4a16a23a7ddc8df565cb |
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| Source note | uspto-grants-1981_03 |
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