1,4-Bis(dihydroquinidine)phthalazine → (2R)-2-(3-bromophenyl)-1,2-propanediol

HRID 1157731노트

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HRID 1157731 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][CH:9]=C)[CH:3]=1.CC[C@@H]1[C@@H]2C[C@H]([C@@H](OC3C4C(=CC=CC=4)C(O[C@@H](C4C=CN=C5C=4C=C(OC)C=C5)[C@@H]4N5C[C@H](CC)[C@@H](CC5)C4)=NN=3)C3C=CN=C4C=3C=[C:25]([O:32]C)C=C4)N(CC2)C1.C([OH:73])(C)(C)C.O>>[Br:1][C:2]1[CH:3]=[C:4]([C@:8]([OH:73])([CH3:9])[CH2:25][OH:32])[CH:5]=[CH:6][CH:7]=1

참가 물질

4

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온도
4 °C

실험 절차

A mixture of 1-bromo-3-(2-propenyl)benzene from step 1 (2.9 g, 15 mmol) and AD-mix-β (Aldrich, 21.0 g) in t-BuOH-H2O (1:1, 150 mL) was vigorously stirred at 4° C. for 16 h. The reaction was quenched with solid Na2SO3 (5.0 g) and diluted with ethyl acetate (150 mL). The aqueous was separated and extracted with ethyl acetate. The combine organic phase was washed with brine, dried and filtered through a short path of silica gel. Removal of the solvent gave essentially pure title compound.

후처리

  1. customThe reaction was quenched with solid Na2SO3 (5.0 g)
  2. additiondiluted with ethyl acetate (150 mL)
  3. customThe aqueous was separated
  4. extractionextracted with ethyl acetate
  5. washThe combine organic phase was washed with brine
  6. customdried
  7. filtrationfiltered through a short path of silica gel
  8. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-086a6a894d3a430c80f8e471244168a9
출처 데이터셋
uspto-grants-2010_10
특허 번호
US07807692B2

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