Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 178511806 | HCID 178511806 | — |
| Solvent | Water | HCID 962 | — |
| Product | D-Histidine | HCID 178511802 | 71.2% |
Reaction Steps
10.0 g of the crude salt from Example 1 were stirred in 15 ml H2O at 80°-90° C. for 30 minutes, cooled below 50° C. and filtered. The solid salt containing 0.03 mole D-histidine tartrate ([α]D +12.17° -C=1.61,H2O) was suspended in 15 ml H2O. With stirring, 0.09 mole (3.6 g) of sodium hydroxide was added and a clear solution was formed. Heat was evolved. Calcium chloride, 0.03 mole (3.33 g) was added and the mixture was stirred at 10°-15° C. for one hour to enable complete precipitation of calcium tartrate. The solid was filtered and washed thoroughly with 3 ml H2O. The filtrate was neutralized with hydrochloric acid 32% (3 ml) to pH=7.5 (isoelectric point) and cooled to 0°-10° C. with stirring for one hour to deposit the free amino acid. The white solid was collected by filtration, washed twice with 3 ml cold methanol: H2O 2:1, then with 2 ml methanol, and dried in vacuo (100° C.) for two hours. D-histidine was obtained in 71.2% yield (3.31 g) with optical purity of 99% ([α]=+39.33). Overall yield from L-histidine=64%. Assay (potentiometric titration, 0.1 NHCl) is 98.99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496955 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-f41e3a350a2146d7aa086b1679e89d0f |
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| Source note | uspto-grants-1996_03 |
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