Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dibromoethane | HCID 7839 | — |
| Edukt | 2-Bromopropene | HCID 11202 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Hex-4-ynal | HCID 10975410 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Methyloct-1-en-6-yn-3-ol | HCID 12653929 | 85% |
Reaktionsschritte
Magnesium (14.4g, 0.6g atom) was dried in a 250ml flask fitted with reflux condenser, mechanical stirrer and addition funnel. After initiation of reaction under dry N2 with about one ml ethylene dibromide in 70ml tetrahydrofuran, 36.0g (0.30 mole) 2-bromopropene was added dropwise at such a rate as to maintain reflux without external heating. The Grignard solution was then stirred until it cooled to room temperature (30 minutes-1 hour). It was then cooled further to -15° in ice-salt, and the total crude 4-hexynal from part (c) above was added dropwise over 15 minutes. The reaction mixture was stirred for 2 hours at room temperature, saturated ammonium chloride solution was added and the product was extracted with ether. There was obtained 23.50g of 2-methyloct-1-en-6-yn-3-ol (85%, based on 4-methyl hexynoate) as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04129599 |
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| Quelldatensatz | uspto-grants-1978_12 |
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| ORD ID | ord-b24878b02837494690d9a7b9ee9fa0c1 |
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| Quellennotiz | uspto-grants-1978_12 |
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