Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Aspartic acid, 1,4-bis(phenylmethyl) ester, 4-methylbenzenesulfonate (1:1) | HCID 2808531 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Dibenzyl L-aspartate | HCID 2808532 | — |
Reaction Steps
19.4 g of the thus-obtained dibenzyl L-aspartate paratoluenesulfonate was suspended in 150 ml of chloroform, to which was added 16 g (0.04 mols) of aqueous 10% sodium hydroxide solution, and stirred at room temperature for 1 hour. Next, the chloroform layer was separated, to which was added 14.7 g (0.04 mols) of O,O′-diparatoluoyl-L-tartaric anhydride, and again stirred at room temperature for 2 hours. The chloroform layer was analyzed through HPLC. Its chart gave two peaks based on O,O′-diparatoluoyl-L-tartaric acid mono-L-(1,2-dibenzyloxycarbonyl)ethylamide (L-L form) of formula (16) and on O,O′-diparatoluoyl-L-tartaric acid mono-D-(1,2-dibenzyloxycarbonyl)ethylamide (L-D form) of formula (17), and the optical purity of the dibenzyl L-aspartate paratoluenesulfonate used in the reaction was found to be 59.0% ee (FIG. 1—column, CAPCELL PAC SG120; eluent, aqueous phosphoric acid solution (pH 2.2)/methanol=38/62 v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706916B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-9f60f315702d478dbb8a006f304eeacd |
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| Source note | uspto-grants-2004_03 |
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