Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl (2R)-2-amino-3-phenylpropanoate;hydrochloride | HCID 11481330 | — |
| Reactant | HCID 178448099 | HCID 178448099 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 178501369 | HCID 178501369 | 50.8% |
Reaction Steps
D-Phenylalanine methyl ester hydrochloride (20 g, 0.092 mol) was suspended in a solution of triethylamine (66 mL) in dichloroethane (100 mL) and the mixture was stirred for 1 hour at room temperature. The organic layer was separated after washing with water and dried over anhydrous sodium sulphate. Trans-4-isopropylcyclohexane carboxylic acid (15.8 g, 0.092 mol) was added to the organic layer followed by LiOH—Al2O3 (5.5 g of LiOH adsorbed on 40.5 g aluminum oxide) and the resulting mixture heated at for 24 hours. The reaction mixture was filtered through a celite bed and washed with 1.5 N HCl, 5% sodium bicarbonate solution and brine. The organic layer was concentrated to yield 15.5 g of N-(trans-4-isopropylcyclohexylcarbonyl)-D-phenylalanine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314955B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-7fe3a0a784d44bc984df5bd0abdf3b36 |
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| Source note | uspto-grants-2008_01 |
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