Ethyl bromoacetate → 4-Cyano-3-fluorophenoxyacetic acid
반응식
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C(=O)([O-])[O-].[K+].[K+].Br[CH2:18][C:19]([O:21]CC)=[O:20]>CC(C)=O>[C:4]([C:3]1[CH:6]=[CH:7][C:8]([O:10][CH2:18][C:19]([OH:21])=[O:20])=[CH:9][C:2]=1[F:1])#[N:5]참가 물질
실험 절차
The mixture of 2-fluoro-4-hydroxybenzonitrile (274 mg, 2.1 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol) and acetone (25 ml) was refluxed for 6 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 1, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethanol and petroleum ether to give 268 mg 4-cyano-3-fluorophenoxyacetic acid as white crystals, mp 150-152° C.
후처리
- temperaturewas refluxed for 6 h
- temperatureAfter cooling
- filtrationthe mixture was filtered
- customto remove potassium carbonate
- concentrationThe filtrate was concentrated under reduced pressure
- additionTo this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added
- extractionextracted three times with ethyl acetate (20 ml each)
- washwashed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customThe residue was recrystallized from ethanol and petroleum ether
출처 및 근거
- ORD 기록
- ord-4e9ef3eccce7472b8f6368b0de377b71
- 출처 데이터셋
- uspto-grants-2007_06
- 특허 번호
- USRE039707E1
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