Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 66936517 | HCID 66936517 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66935901 | HCID 66935901 | 100% |
Reaction Steps
To a solution of phenylmethyl trans-2,5-dimethyl-1-piperazinecarboxylate (enantiomeric mixture) (1.35 g, 5.43 mmol) in dichloromethane (40 mL) at 0° C. was added formaldehyde (0.817 mL, 37% water solution, 10.87 mmol) followed by sodium triacetoxyborohydride (1.726 g, 8.14 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 2 h before being diluted with dichloromethane and washed with 1N NaOH solution. The organics were washed with brine, dried (MgSO4) and evaporated to yield phenylmethyl trans-2,4,5-trimethyl-1-piperazinecarboxylate (enantiomeric mixture) (1.42 g, 100%). Phenylmethyl trans-2,4,5-trimethyl-1-piperazinecarboxylate (enantiomer 1) (480 mg) and phenylmethyl trans-2,4,5-trimethyl-1-piperazinecarboxylate (enantiomer 2) (400 mg) were separated by chiral chromatography. LCMS: (M+H)+: 263.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893056B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-9d87ce1ac94943ccbade5a26e64a02d4 |
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| Source note | uspto-grants-2011_02 |
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