Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Methyl-2-(4-nitrophenyl)propan-1-ol | HCID 22249279 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67546464 | HCID 67546464 | — |
Reaction Steps
To a stirred solution of 2-methyl-2-(4-nitro-phenyl)-propan-1-ol (prepared by the method described in WO02/66470) (200 mg, 1 mmol) in THF (15 mL) was added NaH (43 mg, 60% in oil) at 0° C. The mixture was stirred at 0° C. for 20 min, MeI (0.22 mL, 1.5 mmol) was added and the mixture was stirred for 2 h at 0° C. then overnight at RT. H2O was added and the mixture was extracted with EtOAc. The organic phase was dried, filtered and evaporated to give 1-(2-methoxy-1,1-dimethyl-ethyl)-4-nitro-benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07320992B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-7a35f7e0a3f247b2a64f8c7aab5c0a0c |
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| Source note | uspto-grants-2008_01 |
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