Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenamine, 3,5-bis(trifluoromethyl)- | HCID 9480 | — |
| Reactant | Ethyl (methylthio)acetate | HCID 78199 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19977165 | HCID 19977165 | 103.5% |
Reaction Steps
Freshly prepared tBuOCl (2.2 g, 20 mmol) was added dropwise to a stirred cold (-65 ° C.) solution of 3,5-bis-(trifluoromethyl)aniline (4.58 g, 20 mmol) in anhydrous CH2Cl2 (25 mL). After 10 minutes, neat ethyl (methylthio)acetate (2.68 g, 20 mmol) was added and the mixture; stirred at -65° C. for 1 hr. Triethylamine (2.68 g, 20 mmol) was added and then the mixture was allowed to warm to room temperature. The reaction mixture was quenched with water, the organic layer was separated and then rotary evaporated. The oily residue (6.35 g) was dissolved in hexanes and boiled for several hours and then allowed to cool. The precipitated beige solid was filtered and washed with hexanes to afford 3.67 g of pure (methylthio) indolone intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565483 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-070e6eb76c5041ceba7af9fe3d875eea |
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| Source note | uspto-grants-1996_10 |
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