Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 23368365 | HCID 23368365 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23368468 | HCID 23368468 | — |
Reaction Steps
To a solution of 0.50 g of 3-(2-amino-3-methoxypropoxy)-5-chloro-1,2-benzoisoxazole are added 0.41 g of p-toluenesulfonic acid and 0.34 ml of 37% formalin, and 0.26 g of sodium cyanoborohydride is then added at 15°-20° C., after which they are subjected to reaction at the same temperature for one hour. Water and ethyl acetate are added to the reaction mixture, and the pH is adjusted to 10 with a 10% (w/w) aqueous sodium hydroxide solution and the organic layer is separated. The separated organic layer is washed with a saturated saline solution and dried over anhydrous magnesium sulfate, after which 0.89 ml of a dioxane solution (2.2N) of hydrogen chloride is added. The crystals precipitated are collected by filtration and recrystallized from a mixed solvent of acetone and methanol, to obtain 0.35 g of colorless, crystalline 5-chloro-3-(2-dimethylamino-3-methoxypropoxy)-1,2-benzoisoxazole hydrochloride having a melting point of 163°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05578627 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-3627f8b5ecd340b5af152827e75ab9b3 |
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| Source note | uspto-grants-1996_11 |
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