HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 70239410, compound → HCID 70239495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 70239410 | HCID 70239410 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 70239495 | HCID 70239495 | 44.5% |
Reaction Steps
Methyl N-[(S)-α-methylbenzyl]-(RS)-pipecolate (159 mg) was dissolved in methyl tert-butyl ether (2 ml) at room temperature. To this solution was added a mixture of (2S)-L-(−)-malic acid (120 mg) and methyl tert-butyl ether (2 ml) at room temperature and stirred. The resultant solution was allowed to stand at −20° C. for one day to form crystals. The crystals were separated by filtration and dried to yield a (2S)-L-(−)-malic acid salt of methyl N-[(S)-α-methylbenzyl]-(S)-pipecolate (70.8 mg) in an optical purity of 41% de and a yield of 29%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172234B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-78d36c8b531a440c8d756829a907aed4 |
| Source note | uspto-grants-2001_01 |