Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | heptanohydrazide | HCID 240032 | — |
| Reactant | 6-(Chlorocarbonyl)naphthalen-2-yl acetate | HCID 15724809 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19907933 | HCID 19907933 | 75.4% |
Reaction Steps
In a 200 ml-three-necked flask, 1.77 g (12.3 mM) of heptanohydrazide, 3,23 g (13.0 mM) of 6-acetoxy-2-naphthoyl chloride prepared in the same manner as in Example 3 and 90 ml of dioxane were placed and heated to about 80° C. To the mixture, 5.0 ml of pyridine was added at about 80° C. under stirring, followed by heating to 90°-92° C. and stirring for 1 hour at 90°-92° C. After the reaction, the reaction mixture was cooled on an iced water bath and poured into 350 ml of iced water to precipitate a crystal. The crystal was recovered by filtration, followed by washing with water and recrystallization from a mixture solvent (acetoneethyl acetate) to obtain 3.23 g of N-heptanoyl-N'-(6-acetoxy-2-naphthoyl)hydrazine (Yield: 75.4 %) ##STR137##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05091109 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-0e78f13426954d7d8fda576566d30c21 |
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| Source note | uspto-grants-1992_02 |
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