Hydrochloric Acid → 11-(3,5-Bis(trifluoromethyl) phenoxy)dodecanoic acid
반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]([OH:13])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.Br[CH:17]([CH3:30])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]([OH:29])=[O:28].Cl>[OH-].[Na+]>[F:1][C:2]([F:14])([F:15])[C:3]1[CH:4]=[C:5]([CH:6]=[C:7]([C:9]([F:11])([F:10])[F:12])[CH:8]=1)[O:13][CH:17]([CH3:30])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]([OH:29])=[O:28]참가 물질
5
실험 절차
3,5-Bis(trifluoromethyl) phenol (20.6 g) was dissolved in 1N sodium hydroxide (270 mL). The solution was refluxed under heating for 10 hours. Further, the solution was added with 11-bromododecanoic acid (4.7 g). After the reflux under heating was continued, the reaction solution was left to be cooled. The reaction solution was added with 1N aqueous hydrochloric acid and extracted with ethyl acetate. The resulting organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed. The resulting crystals was washed with hexane and purified by silica gel column chromatography to obtain 11-(3,5-Bis(trifluoromethyl) phenoxy)dodecanoic acid (18.4 g, 50%).
후처리
- temperatureThe solution was refluxed
- temperatureunder heating for 10 hours
- temperatureAfter the reflux
- temperatureunder heating
- waitthe reaction solution was left
- temperatureto be cooled
- extractionextracted with ethyl acetate
- dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
- customthe solvent was removed
- washThe resulting crystals was washed with hexane
- custompurified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-8166c470559342e5b823bd2e576321b5
- 출처 데이터셋
- uspto-grants-2011_02
- 특허 번호
- US07887835B2
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