Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (-)-2-amino-1butanol D-(-)-mandelate | HCID 70562055 | — |
| Reactant | (-)-2-amino-1-butanol L-(+)-mandelate | HCID 131712145 | — |
| Product | Mandelic Acid | HCID 1292 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04260815 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-21b76a262ac3437ea32b580429b9db6b |
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| Source note | uspto-grants-1981_04 |
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