Ethanol → (S)-4-bromo-3-methyl-butyric acid ethyl ester

HRID 1096182노트

반응식

HRID 1096182 반응식
[C:1]([Br:4])(=O)[CH3:2].C[C@@H:6]1[CH2:10][O:9][C:8](=[O:11])[CH2:7]1.[CH3:12]CO>>[CH2:10]([O:9][C:8](=[O:11])[CH2:7][C@H:2]([CH3:12])[CH2:1][Br:4])[CH3:6]

참가 물질

4

반응물 3

HCID 702Ethanol2회HCID 10482Acetyl bromideHCID 11115993(4S)-Dihydro-4-methyl-2(3H)-furanone

생성물 1

HCID 11085055(S)-4-bromo-3-methyl-butyric acid ethyl ester

실험 절차

To EtOH (55 ml) cooled to 0° C. was added acetyl bromide (41 ml, 0.6 mol) dropwise, followed by a solution of (S)-4-methyl-dihydro-furan-2-one (Tetrahedron 1983, 39, 3107; 18.6 g, 0.2 mol) in EtOH (20 ml). The ice bath was removed and the reaction allowed to reach RT. After 2 h of stirring the reaction was concentrated, the residue redissolved in CH2Cl2, washed with sat. aq. NaHCO3 solution, dried (Na2SO4) and concentrated affording (S)-4-bromo-3-methyl-butyric acid ethyl ester (33.6 g, quant). This was redissolved in EtOH (100 ml), cooled to 0° C. and N-benzylglycine ethyl ester (28.2 g, 0.14 mol) and triethylamine (22.4 ml, 0.16 mmol) were added. The reaction was then warmed to 75° C. for 4 d after which time the reaction was concentrated, the residue redissolved in CH2Cl2, washed with sat. aq. NaHCO3 solution, dried (Na2SO4) and concentrated. Purification by flash column chromatography (EtOAc/heptane 5:95) afforded the titled product as a light gold oil (20.3 g, 43%). MS (ISP)=322.2 (M+H)+.

후처리

  1. customThe ice bath was removed
  2. customto reach RT
  3. concentrationwas concentrated
  4. dissolutionthe residue redissolved in CH2Cl2
  5. washwashed with sat. aq. NaHCO3 solution
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-5c3a1feb09684acaa6d95d5ff64c16ec
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08138175B2

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