HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-Methoxy-N-methylcyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-tert-butoxycarbonyl-3-methoxy-2-methylaniline | HCID 10609918 | — |
| Reactant | [2-(Tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketone | HCID 10804518 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | N-Methoxy-N-methylcyclopropanecarboxamide | HCID 15643267 | — |
Reaction Steps
Using the procedure described in Example 9, Part A, 100 mL (130 mmol) of 1.3M sec-butyl lithium in cyclohexane was reacted with N-tert-butoxycarbonyl-3-methoxy-2-methylaniline (15.4 g, 65 mmol) in 100 mL of THF and then with 8.4 g (65 mmol) of N-methoxy-N-methylcyclopropylcarboxamide to give crude [2-(tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketone. This material on treatment with 20 mL of trifluoroacetic acid in 300 mL of methylene chloride for 6 hours gave a material that was chromatographed on silica gel. Eluting with a gradient, toluene→5% EtOAc/toluene, there was obtained 6.4 g (52% yield) of 2-cyclopropyl-4-methoxy-1H-indole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733923 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-34fde6f5003d4e6dab0c33bf86ba9d7f |
| Source note | uspto-grants-1998_03 |