HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-mandelic acid → HCID 70239495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-mandelic acid | HCID 439616 | — |
| Reactant | HCID 70239410 | HCID 70239410 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | (S)-mandelic acid | HCID 439616 | — |
| Product | HCID 70239495 | HCID 70239495 | 57.2% |
Reaction Steps
Methyl N-[(S)-α-methylbenzyl]-(RS)-pipecolate (157 mg) was dissolved in methyl tert-butyl ether (2 ml) at room temperature. To this solution was added a mixture of L-(+)-mandelic acid (86 mg) and methyl tert-butyl ether (2 ml) at room temperature and stirred. The resulting solution was allowed to stand at −20° C. for one day to form a crystal. The crystals were separated by filtration and dried to yield an L-(+)-mandelic acid salt of methyl N-[(S)-α-methylbenzyl]-(S)-pipecolate (79.9 mg) in an optical purity of 73% de and a yield of 23%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172234B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-a781dfaa67ff4b8f983fabb696471456 |
| Source note | uspto-grants-2001_01 |