Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 13015743 | HCID 13015743 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13656090 | HCID 13656090 | — |
Reaction Steps
A mixture of 3.0g (8.2 mmole) of ethyl[[7-chloro-3-(2-fluorophenyl)-1,2-benzisoxazol-6-yl]thio]acetate, 2.5g of a 30% H2O2 solution, 10 ml of formic acid and 50 ml of CH2Cl2 was stirred at room temperature for two hours. The reaction was diluted with water and extracted three times with CH2Cl2. The organics were combined, washed with dilute NaHCO3 and dried over MgSO4. The solution was concentrated at reduced pressure to a yellow oil which solidified to a cream-colored solid, 3.0g (94%) of ethyl[[7-chloro-3-(2-fluorophenyl)-1,2-benzisoxazol-6-yl]sulfinyl]acetate, m.p. 115°-118° C. The solid was recrystallized from ether to afford pale yellow prisms of ethyl[[7-chloro-3-(2-fluorophenyl)-1,2-benzisoxazol-6-yl]sulfinyl]acetate, m.p. 120°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04602028 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-d6201f67c16145d89adaf71aee30c713 |
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| Source note | uspto-grants-1986_07 |
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