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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257660Generated: October 26, 2026

Formaldehyde → Octrizole

https://huagongshe.com/reaction/257660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
ReactantFluorenoneHCID 10241—
ReactantSodium HydroxideHCID 14798—
Reactant2-((2-Nitrophenyl)azo)-4-(1,1,3,3-tetramethylbutyl)phenolHCID 103927—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductOctrizoleHCID 6248581%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262541
Source datasetuspto-grants-1993_11
ORD IDord-ccab13c5456a476d987ab058d540093f
Source noteuspto-grants-1993_11