Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | HCID 15524254 | HCID 15524254 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86758413 | HCID 86758413 | 68% |
Reaction Steps
1.21 g (10.0 mmol) of (−)-1-phenylethylamine and 20 ml of ethanol were added to 2.77 g (10.0 mmol) of (±)-3-(3,4-dichlorophenyl)-3-methoxycarbonylpropionic acid, and the mixture was stirred in a suspended state under heating at a bath temperature of 90 to 110° C. for 4 hours. Then the internal temperature was lowered to 20° C. and the suspension was stirred at this temperature for one hour. The precipitated crystals were filtered out, washed with a small quantity of ethanol and dried to harvest 2.70 g (68.0% yield) of (+)-3-(3,4-dichlorophenyl)-3-methoxycarbonylpropionic acid·(S)-1-phenylethylamine salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06433174B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-d5cf59a237514a109eb4ffec4731a771 |
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| Source note | uspto-grants-2002_08 |
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