4-Chloromandelic acid → 2-(4-Chloro-phenyl)-2-hydroxy-n-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-acetamide

HRID 458248

Reaktionsgleichung

Reaktionsgleichung von HRID 458248
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH2:13][C:14]#[C:15][CH2:16][CH3:17])[CH2:6][O:7][NH2:8].C(N(C(C)C)C(C)C)C.[Cl:27][C:28]1[CH:38]=[CH:37][C:31]([CH:32]([OH:36])[C:33](O)=[O:34])=[CH:30][CH:29]=1.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>CN(C)C=O>[Cl:27][C:28]1[CH:29]=[CH:30][C:31]([CH:32]([OH:36])[C:33]([NH:8][O:7][CH2:6][C:5]2[CH:9]=[CH:10][C:11]([O:12][CH2:13][C:14]#[C:15][CH2:16][CH3:17])=[C:3]([O:2][CH3:1])[CH:4]=2)=[O:34])=[CH:37][CH:38]=1

Komponenten

6

Versuchsvorschrift

O-(3-methoxy-4-pent-2-ynyloxy-benzyl)-hydroxylamine (5.0 g, 21 mmol) and N-ethyldiisopropylamine (Hünig's base, 5.5 g, 42 mmol) are dissolved in 60 ml of N,N-dimethylformamide. 4-chloro-DL-mandelic acid (4.1 g, 22 mmol) and (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP, Castro's reagent, 10 g, 23 mmol) are added successively and the mixture is stirred for 16 h. After pouring the mixture on ice/water, it is extracted with ethyl acetate. The combined organic layer is washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane (4:6)) to obtain 2-(4-chloro-phenyl)-2-hydroxy-N-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-acetamide as yellow resin.

Aufarbeitung

  1. additionAfter pouring the mixture on ice/water, it
  2. extractionis extracted with ethyl acetate
  3. washThe combined organic layer is washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated under reduced pressure
  6. customThe remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane (4:6))

Quellen und Nachweise

ORD-Eintrag
ord-921bf4a08a354f3580fa42e39bc8b254
Quelldatensatz
uspto-grants-2007_03
Patentnummer
US07189873B2

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