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HRID 257651作成日:2026年10月25日

Sulfuric Acid → 2-(2'-Hydroxy-methylphenyl) benzotriazole

https://huagongshe.com/reaction/257651

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Sodium HydroxideHCID 14798—
反応物(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
反応物2-(2-hydroxy-5-methylphenyl)benztriazole N-oxideHCID 13214646—
触媒FluorenoneHCID 10241—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2-(2'-Hydroxy-methylphenyl) benzotriazoleHCID 1358080992.8%

反応手順

To the wet product 12 g (~ 0.4 mol) thus obtained, is added methanol (60 ml), water (30 ml), 97% sodium hydroxide (13.0 g) and 9-fluorenone (0.5 g), and glucose (5.5 g) (0.3 mol) is further added to the mixture over an hour while stirring at 50° to 55° C. The mixture is reacted while stirring at 75° C. (boiling point) for 5 hours. As a result, the N-oxide disappears. The reaction liquor is neutralized with 62% sulfuric acid (19.8 g) to pH 8 to precipitate a crystal. The precipitated crystal is separated by filtration, and the separated crystal is fully washed with water and further with methanol. The washed crystal is then dried, thus obtaining 9.4 g of 2-(2'-hydroxy-methylphenyl) benzotriazole having a melting point of 128 to 130° C. at the yield of 92.8%. One can see that the reduction with aromatic ketones takes over 9 hours to complete. This reduction also required the use of two catalysts and a greater amount of total catalysts.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262541
出典データセットuspto-grants-1993_11
ORD IDord-adf81cdb482147bb8d95ef8e5d349c21
出典メモuspto-grants-1993_11