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2,4-Dichloro-N-methoxy-N-methylbenzamide → 2',4'-Dichlorovalerophenone

HRID 1671327
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HRID 1671327 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](N(OC)C)=[O:10].[Li][CH2:16][CH2:17][CH2:18][CH3:19]>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:10])[CH2:16][CH2:17][CH2:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 118453452,4-Dichloro-N-methoxy-N-methylbenzamideHCID 178418339Butyllithium

생성물 1

HCID 109880862',4'-Dichlorovalerophenone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirring hazy solution of 2,4-dichloro-N-methoxy-N-methylbenzenecarboxamide (1 g, 4.27 mmol), in THF (20 ml) is added BuLi (2.051 ml, 5.13 mmol) in portions. The reaction is stirred for 4 hours at RT and the partitioned between 1M HCl (100 ml) and EtOAc (140 ml). The organic portion is washed with brine, dried over Na2SO4, and concentrated in vacuo. The crude product is purified by ISCO combiflash chromatography eluting with 0 to 100% EtOAc/iso-hexane on a 40 g silica-column to yield 1-(2,4-dichloro-phenyl)-pentan-1-one as a brown oil; 1H NMR (400 MHz, CDCl3) δ 7.45 (1H, d, J 2.0), 7.43 (1H, d, J 7.3), 7.32 (1H, dd, J 7.3, 2.0), 2.94 (2H, t, J 7.4), 1.70 (2H, m), 1.40 (2H, m), 0.95 (3H, t, J 7.3).

후처리

  1. customthe partitioned between 1M HCl (100 ml) and EtOAc (140 ml)
  2. washThe organic portion is washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. customThe crude product is purified by ISCO combiflash chromatography
  6. washeluting with 0 to 100% EtOAc/iso-hexane on a 40 g silica-column

출처 및 근거

ORD 기록
ord-9bf9e07a4e094765acf3743e102ad69e
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994203B2

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