HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 5851, compound → HCID 66735391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 5851 | HCID 5851 | — |
| Reactant | 2,3-Dihydroxybutanedioate | HCID 3806114 | — |
| Reactant | HCID 66735189 | HCID 66735189 | — |
| Product | HCID 66735391 | HCID 66735391 | 6.3% |
Reaction Steps
According to the process disclosed in GB Patent No. 2 225 321, racemic 1-(4-chlorophenyl)-phenylmethyl-piperazine is resolved using 2 molar equivalent amount of (R)-tartaric acid and the tartarate salt having unsatisfactory optical purity obtained after three recrystallizations was neutralized. The thus obtained base was crystallized three times from hexane. The process provided (R)-(−)-1-(4-chlorophenyl)-phenylmethyl-piperazine in the yield of 6.3%. This method is not suitable for the use in the pharmaceutical industry since neither the product purity nor the yield are satisfactory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851627B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-0c5b67c592bd4e59b7821684f7165b0d |
| Source note | uspto-grants-2010_12 |