Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | HCID 18357635 | HCID 18357635 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 12703747 | HCID 12703747 | — |
Reaction Steps
22.32 g of 3-(p-formylphenyl)-1,2-benzisoxazole, 14.03 g of p-chloroaniline and 0.5 g of boric acid in 160 ml of xylene are refluxed for 2 hours, the water formed being distilled off. The mixture is cooled to 60° C., 500 ml of methanol are added and the resulting mixture is further cooled to -10° C. The product which has precipitated is filtered off with suction, washed with 100 ml of cold methanol and dried. This gives 32 g (96.2% of theory) of compound (102) in the form of pale yellow crystals which melt at 164° to 165° C. After recrystallising twice from toluene, pale yellow crystals with a melting point of 164.5° to 165° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04113938 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-e214c028425d4bd1a729bd8acac29ee4 |
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| Source note | uspto-grants-1978_09 |
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