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Ketenes cyclopropanone hemiacetal

Cyclopropanone hemiacetals and hydrate react with ketene to form acetoxy derivatives, e.g. 86 and 87, respectively. 5 15>80) As shown in Scheme 14, the diacetoxy compound 87 may also be obtained from the reaction of cyclopropanone with acetic acid and excess ketene. 83>... [Pg.108]

Cyclopropanone hemiacetals from ketenes and diazo compds. [Pg.210]

Cyclopropanone ethyl hemiacetal was first synthesized by the reaction of ketene and diazomethane 1n ether at -78°C in the presence of ethanol.4 The yield is low (43%) and the reaction 1s hazardous, especially when a large-scale reaction is required. The method described in this procedure for the preparation of cyclopropanone ethyl hemiacetal from ethyl 3-chloropropanoate... [Pg.151]


See other pages where Ketenes cyclopropanone hemiacetal is mentioned: [Pg.4]   
See also in sourсe #XX -- [ Pg.31 ]

See also in sourсe #XX -- [ Pg.31 ]




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Cyclopropanone

Cyclopropanone hemiacetals

Cyclopropanones

Hemiacetal

Hemiacetalization

Ketenes cyclopropanones

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