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HRID 257660作成日:2026年10月26日

Formaldehyde → Octrizole

https://huagongshe.com/reaction/257660

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sulfuric AcidHCID 1118—
反応物FluorenoneHCID 10241—
反応物Sodium HydroxideHCID 14798—
反応物2-((2-Nitrophenyl)azo)-4-(1,1,3,3-tetramethylbutyl)phenolHCID 103927—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物OctrizoleHCID 6248581%

反応手順

Example 11 of U.S. Pat. No. 4,780,541 is duplicated. This is an example of the use of an aldehyde reducing agent and the aromatic ketone 9-fluorenone as a catalyst. Methanol (110 ml), water (20 ml), 97% sodium hydroxide (12.4 g), and 2-nitro-2'-hydroxy-5'-t-octylazobenzene (17.8 g) are mixed and stirred. After adding 9-fluorenone (2.4 g) to the resultant mixture at 65° to 70° C., 80% paraformaldehyde (6 g) is added to the mixture for 4 hours, and then the reaction liquor is further stirred at the boiling point (73° C. ) for 6 hours, thus the reduction reaction having completed. Thereafter, water (50 ml) is added to the reaction liquor, and the reaction liquor is neutralized to pH 8 with 62% sulfuric acid (16 g) to precipitate a crystal. The crystal thus obtained is filtered by suction to separate the crystal, and the separated crystal is fully washed with water and further with methanol. The washed crystal is then dried, thus producing 13.1 g of 2-(2-hydroxy-5-t-octylphenyl)benzotriazole having a melting point of 103° to 105° C. at the yield of 81.0%. One can see that the reaction takes over 10 hours to complete.

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-ccab13c5456a476d987ab058d540093f
出典メモuspto-grants-1993_11