Benzenepropanoic acid → 3-(4-Iodophenyl)propanoic acid
반응식
OS(O)(=O)=O.O.[C:7]1([CH2:13][CH2:14][C:15]([OH:17])=[O:16])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[I:18]I>CC(O)=O.CCOC(C)=O>[I:18][C:10]1[CH:11]=[CH:12][C:7]([CH2:13][CH2:14][C:15]([OH:17])=[O:16])=[CH:8][CH:9]=1참가 물질
실험 절차
A mixture of H2SO4 (1.25 mL), water (12.5 mL) and AcOH (25 mL) in a 250 mL flask and 3-phenylpropanoic acid (3.00 g, 20.0 mmol), iodine (1.40 g, 5.5 mmol) and KIO3 (0.98 g, 4.6 mmol) was added. The reaction was heated to reflux and a solution of iodine (1.40 g, 5.5 mmol) in AcOH (25 mL) was added in portions of 5 mL as the colour of the reaction faded from purple to orange. After 3 hours when no further colour changes appeared the reaction was cooled to room temperature. before quenching with 1M NaHSO3. The reaction was added water and extracted with EtOAc. The organic phases were combined, washed with brine, dried over MgSO4 and concentrated under vacuum. The product (4.15 g, 75%), containing minor impurites of starting material and the ortho-iodinated product, was recrystallised from PE to provide 1.83 g (33%) of the pure and white crystalline product. Rf: 0.10 (EtOAc:hexanes, 1:4); 1HNMR (CDCl3) δ 7.62-7.59 (m, 2H), 6.97-6.95 (m, 2H), 2.92-2.87 (t, 2H, J=7.5 Hz), 2.68-2.63 (t, 2H, J=7.5 Hz); 13CNMR (CDCl3) δ 178.5, 139.7, 137.6, 130.4, 91.6, 35.2, 30.0.
후처리
- temperatureThe reaction was heated
- temperatureto reflux
- custombefore quenching with 1M NaHSO3
- additionThe reaction was added water
- extractionextracted with EtOAc
- washwashed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated under vacuum
- additionThe product (4.15 g, 75%), containing minor impurites of starting material
- customthe ortho-iodinated product, was recrystallised from PE
- customto provide 1.83 g (33%) of the pure and white crystalline product
출처 및 근거
- ORD 기록
- ord-7e0ab8d1f88649c787a49ab8ed3ec86e
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08586607B2
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