Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (2S)-2-[(2-Chloro-5-nitrophenoxy)methyl]pyrrolidine | HCID 17755967 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 17756290 | HCID 17756290 | — |
Reaction Steps
To (S)-2-(2-chloro-5-nitro-phenoxymethyl)-pyrrolidine (4.82 g, 18.77 mmol) in 167 mL CH3CN at RT was added 37% aqueous formaldehyde (7.58 mL) then NaCNBH3 (1.887 g, 30.03 mmol). The reaction was stirred for 1 h, as the reaction pH was adjusted every 10 min to about 7 by adding small amounts of HOAc. The reaction was concentrated to small aqueous volume and dissolved into 2 N NaOH (aq) and Et2O. The layers were separated, and the organic layer was washed twice with 2 N NaOH then extracted twice with 1 N HCl (aq). The combined acidic aqueous layers were basified to pH>12 with solid NaOH and extracted 3× with EtOAc. The EtOAc layers were washed once with 2 N NaOH then once with a mixture of brine and 2 N NaOH, combined, dried over Na2SO4, filtered, and concentrated down to dryness, to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531553B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-8ff3dc4c17894f27a5c1c35271dc5581 |
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| Source note | uspto-grants-2009_05 |
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