Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | (-)-2-amino-1butanol D-(-)-mandelate | HCID 70562055 | — |
| Edukt | (-)-2-amino-1-butanol L-(+)-mandelate | HCID 131712145 | — |
| Produkt | Mandelic Acid | HCID 1292 | — |
Reaktionsschritte
To a portion (1100 mls out of a total of 4800 mls) of the mother liquor plus methanol wash liquor obtained from resolution B, containing about 2.4 moles of a mixture of diastereomers, consisting of about 2.25 moles of (-)-2-amino-1-butanol L-(+)-mandelate and about 0.15 mole of (-)-2-amino-1-butanol D-(-)-mandelate, is added 180 grams of potassium hydroxide (88.8% real; 2.85 moles) to obtain a solution having an initial αD25°C. of +24.7° ("as is", 10 cm cell). The solution is then heated at 115°-116° C. under pressure (40 psi) for 4 hours to obtain a mandelic acid solution having an αD25°C. of -3.0° ("as is", 10 cm cell). The resulting solution is essentially racemized, the negative rotation being due to the presence of the (-)-2-amino-1-butanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04259521 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-22bd61aa15e14d4abc47ef21990ded01 |
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| Quellennotiz | uspto-grants-1981_03 |
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