Diethyl Ether → Methyl 2-benzyloxycarbonylamino-2-methyl-3-oxopropionate

HRID 1994430노트

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HRID 1994430 반응식
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[CH2:23]([O:30][C:31]([NH:33][C:34]([CH3:41])([CH2:39][OH:40])[C:35]([O:37][CH3:38])=[O:36])=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(OCC)C.C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH2:23]([O:30][C:31]([NH:33][C:34]([CH3:41])([CH:39]=[O:40])[C:35]([O:37][CH3:38])=[O:36])=[O:32])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1

참가 물질

6

실험 절차

A solution of 97.7 mg (0.23 mmol) of Dess Martin periodinane reagent (Aldrich) in 1 ml of DCM is slowly added dropwise to a solution of 56 mg (0.21 mmol) of methyl 2-benzyloxycarbonylamino-3-hydroxy-2-methylpropionate in 1 ml of DCM, and the mixture is left to stir at room temperature for 30 min. 5 ml of diethyl ether and a mixture of 4 ml of saturated NaHCO3 and 0.36 g of Na2S2O3.5H2O are then added to the solution. It is stirred for 15 min until the solid has dissolved, and then the ether phase is washed with saturated NaHCO3 and water, dried over MgSO4 and concentrated in vacuo. The crude product is purified by chromatography on 4 g of SiO2 with EtOAc/heptane (gradient 0-50%). 40 mg of the desired aldehyde are obtained.

후처리

  1. waitthe mixture is left
  2. additionare then added to the solution
  3. stirringIt is stirred for 15 min until the solid
  4. dissolutionhas dissolved
  5. washthe ether phase is washed with saturated NaHCO3 and water
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe crude product is purified by chromatography on 4 g of SiO2 with EtOAc/heptane (gradient 0-50%)

출처 및 근거

ORD 기록
ord-2ce7eb1272fa44de9d3d6a3adee6ecee
출처 데이터셋
uspto-grants-2010_01
특허 번호
US07652007B2

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