HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-(tert-butyldimethylsilyloxy)-N-methoxy-N-methylcyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 86642922 | HCID 86642922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(tert-butyldimethylsilyloxy)-N-methoxy-N-methylcyclohexanecarboxamide | HCID 23144601 | 73.4% |
Reaction Steps
4-Hydroxy-N-methoxy-N-methylcyclohexanecarboxamide (7.34 g, 39.2 mmol) in N,N-dimethylformamide (200 mL) was stirred with imidazole (4.80 g, 70.6 mmol) and tert-butylchlorodimethylsilane (7.70 g, 51.0 mmol) at room temperature for one day. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=25/1→4/1 (v/v)) to give the title compound as a colorless oil (8.68 g, yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216999B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-340dcc6da55340cf868b1649c8a47626 |
| Source note | uspto-grants-2015_12 |