Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | HCID 10910383 | HCID 10910383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 65648814 | HCID 65648814 | — |
Reaction Steps
To methyl(2E)-4-bromo-2-methylbut-2-enoate (643 mg, 3.33 mmol) in tetrahydrofuran (6.66 mL) was added dimethylamine (5.00 mL, 9.99 mmol, 2M in THF). The reaction was stirred at 25° C. overnight, then concentrated in vacuo and purified by silica chromatography using 1-8% DCM/MeOH (visualized with potassium permanganate stain). The product was collected and concentrated to afford the desired product as a colorless oil. LRMS (ESI) calc'd for C8H16NO2 [M+H]+: 158, found 158.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993756B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0febc2a45d894386a3a19490bb268e4c |
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| Source note | uspto-grants-2015_03 |
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