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

HRID 559343노트

반응식

HRID 559343 반응식
[C:1]([Br:4])(=O)[CH3:2].C[C@@H:6]1[CH2:10][O:9][C:8](=[O:11])[CH2:7]1.[CH2:12](O)C>>[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 ethanol (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 ethanol (20 ml). The ice bath was removed and the reaction allowed to reach room temperature. After 2 h of stirring the reaction was concentrated, the residue redissolved in dichloromethane, washed with saturated aq. sodium hydrogencarbonate solution, dried (Na2SO4) and concentrated affording (S)-4-bromo-3-methyl-butyric acid ethyl ester (33.6 g, quant). This was redissolved in ethanol (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 dichloromethane, washed with saturated aq. sodium hydrogencarbonate solution, dried (Na2SO4) and concentrated. Purification by flash column chromatography (ethyl acetate/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 room temperature
  3. concentrationwas concentrated
  4. dissolutionthe residue redissolved in dichloromethane
  5. washwashed with saturated aq. sodium hydrogencarbonate solution
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3225ce87bb9e4581b6654c6a7a1616a8
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08063042B2

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