Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitropropane | HCID 398 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 18357643 | HCID 18357643 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18357635 | HCID 18357635 | — |
Reaction Steps
115.8 g of 2-nitropropane are introduced at about 30° C. into a solution of 23.13 g of sodium in 2,700 ml of anhydrous ethanol. The mixture is stirred for a further one hour and a solution of 288.1 g of 3-(p-bromomethyl-phenyl)-1,2-benzisoxazole in 350 ml of dimethylformamide is now added. Subsequently, the reaction mixture is warmed to 50° C., then stirred for 20 hours without external warming and finally cooled to -10° C. The product which has precipitated is filtered off with suction, washed with cold methanol and dried. This gives 107.4 g (48.1% of theory) of 3-(p-formylphenyl)-1,2-benzisoxazole in the form of a pale yellow powder with a melting point of 117° to 117.5° C. After recrystallising twice from ligroin, small, virtually colourless, glossy needles are obtained which melt at 117° to 117.5° C.
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-5946e25df71e4db6a0065dbbcd73a9da |
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| Source note | uspto-grants-1978_09 |
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