HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485716Erstellt: 26. Oktober 2026
2,3,4,5,6-Pentafluorobenzyl Alcohol → pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate
https://huagongshe.com/reaction/485716
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,3,4,5,6-Pentafluorobenzyl Alcohol | HCID 9923 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)cyclopropane-carboxylic acid | HCID 18599060 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate | HCID 131714314 | 73% |
Reaktionsschritte
A solution of 4.12 g of dicyclohexylcarbodiimide in 40 ml of methylene chloride was added at 0° C. to a mixture of 3 g of (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylic acid, 30 ml of methylene chloride, 3.96 g of pentafluorobenzyl alcohol and 100 mg of 4-dimethylaminopyridine and the mixture was stirred at 20° C. for 16 hours and was filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 9-1 hexane-ethyl acetate mixture yielded 4.78 g of pentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate with a specific rotation of [α]D20 =-23° (c=0.5% in chloroform).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04537897 |
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| Quelldatensatz | uspto-grants-1985_08 |
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| ORD ID | ord-45c6e0aa1d6c4d56b6c6cbcaf5f003a5 |
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| Quellennotiz | uspto-grants-1985_08 |
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