HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20001Erstellt: 25. Oktober 2026
Tetrakis(hydroxymethyl)phosphonium chloride → 2,2-Dimethoxyethylcyclopent-3-enol
https://huagongshe.com/reaction/20001
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrakis(hydroxymethyl)phosphonium chloride | HCID 31298 | — |
| Edukt | 4-(2,2-Dimethoxyethyl)hepta-1,6-dien-4-ol | HCID 86614113 | — |
| Katalysator | HCID 178425456 | HCID 178425456 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | 2,2-Dimethoxyethylcyclopent-3-enol | HCID 67306500 | — |
Reaktionsschritte
A solution of 4-(2,2-dimethoxyethyl)hepta-1,6-dien-4-ol (28 g, 140 mmol) in DCM (2L) was charged to a 3 L RB flask. Dry argon was bubbled through the solution for 30 minutes. Grubbs second generation catalyst (5.9 g, 7.0 mmol) was added and the reaction was allowed to stir under argon for 15 hours. The reaction was quenched with a solution of tetrakis-(hydroxymethyl)phosphonium chloride (27 g, 140 mmol) in isopropanol (200 mL) and 10 N NaOH (14 mL), and stirred for 15 hours. The reaction was diluted with water (1 L) and poured into a seperatory funnel. The DCM layer was separated and the aqueous was extracted with DCM (3×100 mL). The combined organics were concentrated to a dark oil which was purified by flash chromatography on a 330 g ISCO column eluting by gradient hexanes to 20% EtOAc/ hexanes over a 50 minute period. Product fractions were combined to afford the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745484B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-b35f1b7b6a54453898bc9fec0b4f2792 |
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| Quellennotiz | uspto-grants-2010_06 |
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