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HRID 328752作成日:2026年10月24日

Piperidine → Ethyl 2-(4-oxo-4H-naphtho[1,2-b]pyran-2-yl)cyclopropane carboxylate

https://huagongshe.com/ja/reaction/328752

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Ethyl 2-formylcyclopropanecarboxylateHCID 89334—
反応物HCID 12715524HCID 12715524—
溶媒TolueneHCID 1140—
生成物Ethyl 2-(4-oxo-4H-naphtho[1,2-b]pyran-2-yl)cyclopropane carboxylateHCID 21440282—

反応手順

A mixture of 12.4g of 1'-hydroxy-2-(methylsulfinyl)-2'-acetonaphthone, 7.1g of ethyl 2-formyl-1-cyclopropane carboxylate, 250ml of toluene and 0.5ml of piperidine was refluxed for 8 hrs. The toluene was then removed under reduced pressure, and the oily residue was recrystallized from Skelly B with the aid of charcoal, mp. 106°-07.5°; yield 6.5g (42%); λ max mμ (ε) 219 (50,000), 259 (36,800), 327 (3,990), 341 (4,100); ν max 760 (m), 825 (ms), 1195 (s), 1640 (s), 1650 (s), 1730 (s) cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04018798
出典データセットuspto-grants-1977_04
ORD IDord-5e5375d87fc248c5bdab84e5a8b04f9c
出典メモuspto-grants-1977_04