Hydrochloric Acid → benzhydryl (2R)-hydroxy-4-phenylbutyrate

HRID 1032983

Reaktionsgleichung

Reaktionsgleichung von HRID 1032983
[OH:1][C@H:2]([CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:3]([O:5]CC)=[O:4].[OH-].[Li+].Cl.[C:19]1([C:25]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[N+]=[N-])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>CO>[OH:1][C@H:2]([CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:3]([O:5][CH:25]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:4]

Komponenten

6

Versuchsvorschrift

Dissolve (R)-2-hydroxy-4-phenylbutyric acid, ethyl ester (4.16 g, 20 mmol) in methanol (40 mL). Add 1N lithium hydroxide (25 mL, 25 mmol) and stir under an atmosphere of argon for 3.5 hours. Acidify with 1N hydrochloric acid (25 mL), saturate with sodium chloride and extract with ethyl acetate (3×25mL). Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Take up the residue in methylene chloride (20 mL) and add diphenyldiazomethane (3.36 g, 17.3 mmol). Stir overnight and wash with saturated sodium hydrogen carbonate (2X). Dry (MgSO4), evaporate the solvent in vacuo and recrystallize (methylene chloride/hexane then again with cyclohexane) to give (R)-2-hydroxy-4-phenylbutyric acid, diphenylmethyl ester as white needles (2.3 g, 38%); mp 82°-84° C.

Aufarbeitung

  1. concentrationsaturate with sodium chloride
  2. extractionextract with ethyl acetate (3×25mL)
  3. dry with materialCombine the organic phases, dry (MgSO4)
  4. customevaporate the solvent in vacuo
  5. stirringStir overnight
  6. washwash with saturated sodium hydrogen carbonate (2X)
  7. dry with materialDry (MgSO4)
  8. customevaporate the solvent in vacuo
  9. customrecrystallize (methylene chloride/hexane

Quellen und Nachweise

ORD-Eintrag
ord-6ee2a9f2f73749b68e9f44a751fe5e7a
Quelldatensatz
uspto-grants-1994_05
Patentnummer
US05308841

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