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HRID 1808672作成日:2026年10月26日

Methyl cyanoacetate → Indole

https://huagongshe.com/reaction/1808672

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl cyanoacetateHCID 7747—
反応物PiperidineHCID 8082—
反応物1H-Indole-3-carboxaldehyde, 1-methyl-2-phenyl-HCID 74468—
溶媒MethanolHCID 887—
生成物IndoleHCID 798263.8%

反応手順

To 120 ml of methanol were added 23.5 g (0.10 mol) of 1-methyl-2-phenyl-1H-indole-3-carbaldehyde and 11.9 g (0.12 mol) of methyl cyanoacetate to produce a mixture. Subsequently, 2.5 g (0.03 mol) of piperidine was added to the mixture, reacted under reflux for 6 hours, and cooled to room temperature to precipitate a crystal. The obtained crystal was washed with a small amount of methanol, and then dried to give 30.9 g of a light-yellow crystalline indole compound A having a structure of the general Chemical Formula (1) in which R1 was methyl group and R2 was methyl group. The melting point of the obtained indole compound A was 193.7° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08361625B2
出典データセットuspto-grants-2013_01
ORD IDord-49669eb5cbd143bb9afba59f582bd187
出典メモuspto-grants-2013_01