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HRID 2603作成日:2026年10月25日

Diethanolamine → Tris-(8-di-(2-hydroxyethyl)aminocarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:5,4-d']-bis(1,3)oxathiol-4-yl)methanol

https://huagongshe.com/reaction/2603

反応式

関与物質

役割名称HCID仕込み量
反応物DiethanolamineHCID 8113—
反応物Tris-(8-chlorocarbonyl-2,2,6,6-tetramethyl-benzo[1,2-d:5,4-d']-bis(1,3)oxathiol-4-yl)methanolHCID 88240526—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物Tris-(8-di-(2-hydroxyethyl)aminocarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:5,4-d']-bis(1,3)oxathiol-4-yl)methanolHCID 8824217063.4%

反応手順

Tris-(8-chlorocarbonyl-2,2,6,6-tetramethyl-benzo[1,2-d:5,4-d']-bis(1,3)oxathiol-4-yl)methanol (0.80 g, 0.80 mmol) was dissolved in benzene (200 mL). A solution of of bis(2-hydroxyethyl)amine (8.0 g, 48 mmol) in water (200 mL) was added and after vigorous stirring overnight, the mixture was transferred to a separatory funnel. The aqueous layer was removed and the remaining solid plus the benzene layer was evaporated, dissolved in methanol and passed through a short column (neutral alumina). After elution of unwanted materials with acetonitrile, the amide was eluted with methanol. After evaporation, the product was stirred with water (50 mL) at 40° C. for 2 h and then isolated by filtration. After drying, 0.60 g (60%) of the pure amide was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728370
出典データセットuspto-grants-1998_03
ORD IDord-b9d46f1258cf4095bcf66afa8b7bb539
出典メモuspto-grants-1998_03