Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 1-Bromo-4-methoxy-2-methyl-3-nitrobenzene | HCID 11357012 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59133095 | HCID 59133095 | — |
Reaction Steps
To a solution of 1-bromo-4-methoxy-2-methyl-3-nitrobenzene (1.400 g, 5.68 mmol) and 1,1-dimethoxy-N,N-dimethylmethanamine (0.884 mL, 6.657 mmol) in DMF (10.0 mL) was added pyrrolidine (0.555 mL, 6.656 mmol) and the mixture was heated to at 110° C. for 4 h. The DMF was removed and the residue was recrystallized from DCM:methanol (1:6) mixture to afford 1-[(E)-2-(6-bromo-3-methoxy-2-nitrophenyl)vinyl]pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700594B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-ccab095badcb43c0839644147190b534 |
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| Source note | uspto-grants-2010_04 |
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