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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257660생성일: 2026년 10월 25일

Formaldehyde → Octrizole

https://huagongshe.com/reaction/257660

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sulfuric AcidHCID 1118—
반응물FluorenoneHCID 10241—
반응물Sodium HydroxideHCID 14798—
반응물2-((2-Nitrophenyl)azo)-4-(1,1,3,3-tetramethylbutyl)phenolHCID 103927—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물OctrizoleHCID 6248581%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262541
출처 데이터셋uspto-grants-1993_11
ORD IDord-ccab13c5456a476d987ab058d540093f
출처 메모uspto-grants-1993_11