Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methylpyrrolidine | HCID 13003 | — |
| Reactant | 2-Fluoro-5-nitroaniline | HCID 67785 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 62508285 | HCID 62508285 | — |
Reaction Steps
5 g (32.03 mmol) of 2-fluoro-5-nitroaniline and 4.9 ml (48.04 mmol) of 2-methylpyrrolidine (racemic) are placed in a screw reactor. The reactor is closed and the mixture is heated at 100° C. for 5 h. After cooling, the mixture is taken up with 100 ml of water and 100 ml of dichloromethane. The organic phase is separated, washed with 50 ml of a saturated solution of sodium chloride, dried over magnesium sulphate and then concentrated under reduced pressure. The resulting product is used as it is in the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143248B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-bd5430149e4043088111313661e9afcd |
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| Source note | uspto-grants-2012_03 |
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