3-Phenyl-and 3-(p-methoxyphenyl)-7,8-dihydroxy and -6,7-dihydroxychromenones were prepared from ethyl 3-oxo-2-phenylpropanoate, ethyl 3-oxo-2-(4-methoxyphenyl)-propanoate and the trihydroxy benzenes in H 2 SO 4 . 3-Aryl-7,8-and3-aryl-6,7-dihydroxy-2H-chromenones reacted with the bis-dihalides of pol
The synthesis of novel crown ethers
✍ Scribed by D.N. Reinhoudt; R.T. Gray
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 189 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Che synthesis and chemistry of macrocyclic polyethers are currently receiving a great deal of attention. Very recently Cram and co-workers 132 have reported the synthesis of two crown ethers (3,~ and QJ). We have prepared two series of novel crown ethers in which respectively, the 1,3and 2,5-positions of a benzene and a furan ring are linked via a polyethylene glycol chain. As 3,~ and Q are members of these series, the communications of Cram et al. have prompted us to dis. close the preliminary results of our work. A series of disodium or dipotassium polyethylene glycolates (derived from 2s) were reacted with equimolar amounts of 1,3-bis(bromomethyl)benzene (1) in apolar solvents without using high dilution conditions (0.1 cient to effect complete ,-;_ 0 L 3 M concentration) . Reaction times of 1 to 3 hours at 110 T were suffi- conversion of the starting materials.
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