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HRID 27948作成日:2026年10月25日

9-Amino-12-hydroxy-9,10-dihydro-9,10-ethanoanthracene → 9,10-Dihydro-9,10-methanoanthracene-9-carboxaldehyde

https://huagongshe.com/reaction/27948

反応式

関与物質

役割名称HCID仕込み量
反応物9-Amino-12-hydroxy-9,10-dihydro-9,10-ethanoanthraceneHCID 12404136—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物9,10-Dihydro-9,10-methanoanthracene-9-carboxaldehydeHCID 12404141100.5%

反応手順

To a solution of 9-amino-12-hydroxy-9,10-dihydro-9,10-ethanoanthracene (3.0 g) in acetic acid (240 ml) was added a solution of sodium nitrite (6.7 g) in water (120 ml) at 2°-5° C., and the resulting mixture was stirred at the same temperature for 1 hour and at 95°-105° C. for 5 hours. The reaction mixture was diluted with water and extracted with benzene. The benzene layer was washed with water, dried over sodium sulfate and evaporated to dryness to give crude crystals of 9-formyl-9,10-dihydro-9,10-methanoanthracene (2.8 g), which were recrystallized to give colorless crystals (2.45 g). M.P. 99°-100° C. Further, purification by recrystallization gave analytically pure 9-formyl-9,10-dihyfro-9,10-methanoanthracene, M.P. 102.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04224344
出典データセットuspto-grants-1980_09
ORD IDord-e4ea9ed5834c464ba120c7a9f98353ef
出典メモuspto-grants-1980_09