HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128492Generated: October 25, 2026
(-)-2-amino-1butanol D-(-)-mandelate → (-)-Mandelic acid
https://huagongshe.com/reaction/128492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (-)-2-amino-1butanol D-(-)-mandelate | HCID 70562055 | — |
| Solvent | Water | HCID 962 | — |
| Product | (-)-Mandelic acid | HCID 11914 | 72.6% |
Reaction Steps
A portion of the (-)-2-amino-1-butanol D-(-)-mandelate wet cake (155 grams "as is"--90.3% pure; 0.58 mole) from resolution A is dissolved in water (125 mls) at 50°-55° C. and the resulting solution is distilled under vacuum to remove 48.5 mls of methanol and water. The concentrated solution is treated with 37% hydrochloric acid (60 mls) and the acidified solution is cooled to -5° C. over about 5 hours to crystallize D-(-)-mandelic acid from the solution. The crystals are isolated by filtration, washed twice with ice cold (0°-5° C.) water (20 mls), twice with hexane (20 mls), and dried at 60° C. to obtain 64.1 grams of D-(-)-mandelic acid (72.6% of theoretical; m.p. 131°-133° C.; [α]D25 =-154.1° (C=2. H2O)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259521 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-132d99b23ce84ba99ad73af6c75c17ee |
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| Source note | uspto-grants-1981_03 |
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