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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3,4,5,6-Pentafluorobenzyl AlcoholHCID 9923—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt(1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)cyclopropane-carboxylic acidHCID 18599060—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produktpentafluorobenzyl (1R,trans) 2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylateHCID 13171431473%

Reaktionsbedingungen

Temperatur20 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04537897
Quelldatensatzuspto-grants-1985_08
ORD IDord-45c6e0aa1d6c4d56b6c6cbcaf5f003a5
Quellennotizuspto-grants-1985_08