Dimethylformamide → HCID 17986946, 화합물

HRID 1376279노트

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HRID 1376279 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=O)=[CH:4][CH:3]=1.C[N:15](C=O)C.C(Cl)(=O)C(Cl)=O>C(Cl)(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([NH2:15])=[O:13])=[CH:4][CH:3]=1

참가 물질

5

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온도
0 °C

실험 절차

To a solution of 4-(4-fluorophenyl)-butyric acid (6.7 g) in chloroform (15 ml) at 0° C. was added 0.1 ml DMF followed by the addition of oxalyl chloride (3.35 ml) over 20 min. The solution was stirred for 2 h then concentrated. The crude acid chloride was dissolved in chloroform (150 ml) and cooled to 0° C., whereupon concentrated ammonia solution (6 ml) was added over 15 min and the resulting solution stirred for 2 h. The reaction mixture was washed with water and the organic phase dried (MgSO4) and concentrated in vacuo. The crude product was chromatographed over silica using a gradient elution from ether to 2:1 acetone/ether to yield the title compound (2.86 g, 43%). 1H-NMR (CDCl3) δ 1.96 (2H, app q), 2.21 (2H, t), 2.65 (2H, t), 5.41 (2H, br s), 6.96 (2H, m), 7.14 (2H, m). MS(APCI+)M+1=182, C10H12FNO requires 181.

후처리

  1. concentrationthen concentrated
  2. dissolutionThe crude acid chloride was dissolved in chloroform (150 ml)
  3. additionwas added over 15 min
  4. stirringthe resulting solution stirred for 2 h
  5. washThe reaction mixture was washed with water
  6. dry with materialthe organic phase dried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customThe crude product was chromatographed over silica using
  9. washa gradient elution from ether to 2:1 acetone/ether

출처 및 근거

ORD 기록
ord-e48a1a58147442adb067efa410fb1efe
출처 데이터셋
uspto-grants-2007_01
특허 번호
US07169924B2

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