HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-t-butoxycarbonyl-N-methylamino-2-hydroxy-5-methylhexane | HCID 19753986 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexane | HCID 19753925 | 88.5% |
Reaction Steps
To a solution of 1-(N-t-butoxycarbonyl-N-methylamino-2-hydroxy-5-methylhexane (2.45 g) and triethylamine (3.03 g) in dimethyl sulfoxide (20 ml) was added sulfur trioxide pyridine complex (4.77 g) under ice-bath cooling. After the mixture was stirred at ambient temperature overnight, the reaction mixture was poured into ice-water (100 ml). The mixture was extracted with diethyl ether (100 ml×2). The extract was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (20% ethyl acetate in n-hexane as eluent) to give 1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexane (2.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05142048 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-3a53f2e7437740898bcacfe1402b0681 |
| Source note | uspto-grants-1992_08 |