Ethylene Oxide → 18-Crown-6

Preparation of the cyclic tetramer of ethylene oxide by the cyclization of ethylene oxide over an organo-metallic catalyst, for example triethyl aluminum, ethyl zinc butoxide or diethyl magnesium, is taught by Stewart, et al. in British patent Specification No. 785,229. C. J. Pedersen in U.S. Pat. No. 3,687,978 teaches the preparation of macrocyclic polyethers by the reaction of vicinal aromatic diols with α,ω-dihalides of polyoxyalkylene materials and sodium hydroxide in 1-butanol solvent. Pedersen also describes the preparation of the cyclic oxyethylene hexamer by the autoelimination reaction of the α,ω-chlorohydrin of hexaethylene glycol in the presence of potassium t-butoxide in a 1,2-dimethoxy ethylene solvent in U.S. Pat. No. 3,562,295. The ethylene oxide cyclic hexamer is produced in a very low yield of 1.8%. Dale et al. describe a base catalyzed preparation in Chem. Comm. 670 (1971). There, glycols and glycol ditosylates are condensed with potassium t-butoxide in benzene in about 15-35% yields.

ORDレコード

ord-f0d07f94a437405a884264c040ce6574

出典データセット

uspto-grants-1978_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04113739