Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86745339 | HCID 86745339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86745338 | HCID 86745338 | — |
Reaction Steps
A solution of 5-[(2-chloro-α,α,α,6-tetrafluro-p-tolyl)oxy]-2-indolinone (16.8 g, 0.0485 mol) in toluene is treated in a single portion with a 60% sodium hydride dispersion in mineral oil (2.13 g, 0.0534 mol NaH) at 60° C., stirred for 30 minutes, treated dropwise with a solution of dimethylsulfate (5.1 mL, 0.0534 mol) in toluene over a 20 minute period at 60° C., stirred for 2 hours, cooled to room temperature and diluted with a mixture of ethyl acetate and water. The phases are separated, the organic phase is washed with brine and the aqueous phases are combined and further extracted with ethyl acetate. All organic phases are combined, dried over MgSO4, and concentrated in vacuo to give a light brown semi-solid residue. Trituration under a mixture of 3-5% ethyl acetate in hexane and filtration yields the title product as a light pink solid, 13.45 g (77%), mp 111-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05076835 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-0852f11dde444259869f76af32be5be2 |
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| Source note | uspto-grants-1991_12 |
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