Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Fluorenone | HCID 10241 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(2H-Benzotriazol-2-yl)-4,6-bis(tert-pentyl)phenol N-oxide | HCID 11143110 | — |
| Solvent | Water | HCID 962 | — |
| Product | UV-328 | HCID 33263 | 92.8% |
Reaction Steps
2-(2-hydroxy-3,5-di-t-amylphenyl)benzotriazole-N-oxide 23.2 g was added to a mixture of n-butanol 60 g, water 12 g and 97% sodium hydroxide 16.5 g, and 9-fluorenone 2.0 g was further added to the resultant mixture. The resultant mixture was heated to 80° C., and was further stirred at 80°~85° C. for 2.5 hours, thus the reduction reaction being completed. The reaction liquor was treated in the same manner as in Example 17 to recover butanol, and 1.8 g of 9-fluorenone catalyst was recovered as a fraction at 120°~130° C. under vacuum of 2~3 mmHg. After recovering the catalyst, the remaining material was washed with methanol to produce the desired product, i.e. 20.5 g of 2-(2-hydroxy-3,5-di-t-amylphenyl)benzotriazole having a melting point of 79°~80° C. at the yield of 92.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943637 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-57972ed3ec024a77926e8f7e74e76af0 |
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| Source note | uspto-grants-1990_07 |
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