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Triethylsilane → 4-(4-Bromo-2-methylphenyl)butanoic acid

HRID 735638
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HRID 735638 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[C:4]([CH3:15])[CH:3]=1.C([SiH](CC)CC)C>C(O)(C(F)(F)F)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[C:4]([CH3:15])[CH:3]=1
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참가 물질

4

반응물 2

HCID 12052TriethylsilaneHCID 247270004-(4-Bromo-2-methylphenyl)-4-oxobutanoic acid

생성물 1

HCID 578426164-(4-Bromo-2-methylphenyl)butanoic acid수율 42%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
90 °C

실험 절차

To a solution of 55A (542 mg, 2 mmol) in TFA (5 mL) was added triethylsilane (0.8 mL, 5 mmol) and the mixture heated at 90° C. for 7 h. The reaction was quenched with 1N NaOH (20 mL) and washed with EtOAc (20 mL). Aqueous layer was acidified to pH 1 with 1N HCl and extracted with EtOAc (2×20 mL). The combined organics were washed with brine (10 mL) and dried (MgSO4). The organic layer was concentrated in vacuo and the residue purified by flash chromatography (0-100% EtOAc/Hexane) to afford 55B (216 mg, 42%) as an oil. 1H NMR (400 MHz, CDCl3) δ ppm 0.98 (t, 3 H) 2.42 (q, 2 H) 2.73 (t, 2 H) 4.10 (t, 2 H) 6.82 (d, 1 H) 7.02 (d, H) 7.09 (t, 2 H) 7.15 (t, 1 H) 7.36 (d, 1 H) 7.58-7.63 (m, 1 H).

후처리

  1. customThe reaction was quenched with 1N NaOH (20 mL)
  2. washwashed with EtOAc (20 mL)
  3. extractionextracted with EtOAc (2×20 mL)
  4. washThe combined organics were washed with brine (10 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationThe organic layer was concentrated in vacuo
  7. customthe residue purified by flash chromatography (0-100% EtOAc/Hexane)

출처 및 근거

ORD 기록
ord-e768230ac9a444d6b9ec18c387226f20
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592331B2

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