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HRID 54602作成日:2026年10月27日

1,3,3-Trimethyl-2-methyleneindoline → 1,3,3-Trimethyl-6'-morpholinospiro[indoline-2,3'-[3H]-naphtho[2,1-b]pyran]

https://huagongshe.com/reaction/54602

反応式

関与物質

役割名称HCID仕込み量
反応物1,3,3-Trimethyl-2-methyleneindolineHCID 8351—
反応物Ethyl orthoformateHCID 31214—
反応物4-Morpholino-2-naphtholHCID 10988042—
溶媒Diethyl EtherHCID 3283—
生成物1,3,3-Trimethyl-6'-morpholinospiro[indoline-2,3'-[3H]-naphtho[2,1-b]pyran]HCID 1586883734%

反応手順

A mixture of 4-morpholino-2-naphthol (0.47 g;0.002 mol), prepared as in 2(b) above, 1,3,3-trimethyl-2-methyleneindole (0.8 g;0.0022 mol) and triethylorthoformate (10.0 ml) was stirred under nitrogen and heated to reflux for 18 hrs. The resulting purple solution was cooled and evaporated to remove the excess triethylorthoformate and the residue flash chromatographed over silica (40% diethyl ether in hexane) to yield an orange gum (0.28 g; yield 34%). Trituration of the gum with diethyl ether afforded the 1,3,3-trimethyl-6'-morpholinospiro [indoline-2,3'-[3H]-naphtho[2,1-b]pyran having the structure shown below as a pale brown solid, m.pt 191°-194° C. ##STR20##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05623005
出典データセットuspto-grants-1997_04
ORD IDord-65b5dd14fecf47bd973f6544bcddcf9c
出典メモuspto-grants-1997_04