Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Chloro-6-fluoro-3-methylanisole | HCID 2773658 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 86642296 | HCID 86642296 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17989205 | HCID 17989205 | 53.4% |
Reaction Steps
17.6 g (100.8 mmol) of 2-chloro-6-fluoro-3-methylanisole is dissolved in 880 ml of toluene. After 27.8 g (403.2 mmol) of isobutyric acid nitrite is added, 302.4 ml (151.2 mmol) of a 0.5 molar solution of potassium hexamethyl disilazide in toluene is added in drops within 40 minutes (temperature increase to 27° C.). After 19 days of stirring at room temperature, the batch is mixed with 300 ml of water and 400 ml of ethyl acetate, and then acidified with 10% sulfuric acid until a pH of 4 is reached. The aqueous phase is shaken with 200 ml of ethyl acetate. The combined organic extracts are washed with water and twice with saturated NaCl solution ad then dried. After spinning-in and chromatography on silica gel (mobile solvent ethyl acetate/hexane), 12.01 g (53.4%) of the desired compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097627B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-d1ea5f8dfa00471090a169f357309261 |
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| Source note | uspto-grants-2012_01 |
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