HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 5-Tert-butyl-2-methoxy-3-trimethylsilanyloxymethyl-phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Amino-5-tert-butyl-2-methoxyphenyl)methanol | HCID 58366895 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Tert-butyl-2-methoxy-3-trimethylsilanyloxymethyl-phenylamine | HCID 58493980 | — |
Reaction Steps
3.03 g (3-amino-5-tert-butyl-2-methoxy-phenyl)-methanol and 2.4 g imidazole are dissolved in 20 ml of tetrahydrofuran and 2.75 ml trimethylsilyl chloride are added dropwise thereto. The mixture is stirred for 2 hours at ambient temperature, the solvents are eliminated in vacuo and the residue is divided between 10% aqueous potassium carbonate solution and ethyl acetate. The aqueous phase is extracted with ethyl acetate and the combined organic phases are washed with saturated sodium chloride solution. After drying with magnesium sulphate the solvents are eliminated in vacuo and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 95:5 to 50:50).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08686022B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-50a7c7795a154655ab5135856a7a4dc1 |
| Source note | uspto-grants-2014_04 |