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HRID 2106629作成日:2026年10月25日

Sodium Hydroxide → 9'-methoxy-1,3,3-trimethylspiro [benz[g] indoline-2,3'-[3H] naphth [2,1-b][1,4] oxazine]

https://huagongshe.com/reaction/2106629

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物7-Methoxy-1-nitrosonaphthalen-2-olHCID 2833080—
反応物1,2,3,3-tetramethyl-3H-benz[g] indolium iodideHCID 13627405—
溶媒HexaneHCID 8058—
生成物9'-methoxy-1,3,3-trimethylspiro [benz[g] indoline-2,3'-[3H] naphth [2,1-b][1,4] oxazine]HCID 14848353—

反応手順

To a solution of 1.05 grams (3.0 mmole) of 1,2,3,3-tetramethyl-3H-benz[g] indolium iodide in 15 milliliters (ml) of hexane at 25° C. was added 10 ml (50 mmole) of 20% sodium hydroxide. The two phase mixture was stirred vigorously under nitrogen for about 30 minutes. The organic layer was separated, transferred to a reaction flask equipped with a reflux condenser and diluted with 15 ml of absolute ethanol. To this solution was added 0.61 grams (3.0 mmole) of 7-methoxy-1-nitroso-2-naphthol and the resulting reaction mixture refluxed under nitrogen for about 6 hours. The reaction mixture was cooled, the volume reduced under vacuum and 0.29 grams (0.71 mmole) of the product, 9'-methoxy-1,3,3-trimethylspiro [benz[g] indoline-2,3'-[3H] naphth [2,1-b][1,4] oxazine] was obtained as yellow-orange crystals. A solution of the crystals dissolved in ethanol or toluene was colorless. The solution turned blue when irradiated with ultraviolet light.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04931219
出典データセットuspto-grants-1990_06
ORD IDord-e650af34ceed47e782b3d534b444c563
出典メモuspto-grants-1990_06