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Methyl 3-bromo-5-ethylbenzoate → HCID 67324020, 화합물

HRID 1397263
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HRID 1397263 반응식
Br[C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH2:12][CH3:13])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[Cu](C#N)[C:15]#[N:16]>CN(C=O)C>[C:15]([C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH2:12][CH3:13])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6])#[N:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67325611Methyl 3-bromo-5-ethylbenzoateHCID 178418260HCID 178418260, 화합물

생성물 1

HCID 67324020HCID 67324020, 화합물수율 39%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

The product methyl 3-bromo-5-ethylbenzoate (0.9 g, 3.7 mmol) was dissolved in dry DMF (50 mL) and copper cyanide (0.84 g, 9.43 mmol) was added. The reaction mixture was heated to 150° C. under argon atmosphere for 12 h (monitored by TLC; petroleum ether/EtOAc 9:1). The reaction mixture was allowed to come to room temperature and then quenched with saturated ammonium chloride solution. The reaction mixture was diluted with EtOAc and filtered through a Celite bed. The filtrate was diluted with EtOAc and the organic layer was washed with water and brine. The solvent was evaporated under reduced pressure. The crude product was purified by column chromatography (silica 60-120 mesh, eluent 5% EtOAc in petroleum ether) to get methyl 3-cyano-5-ethylbenzoate (0.27 g, yield 39%) as colorless liquid, which was carried through without further purification.

후처리

  1. customto come to room temperature
  2. customquenched with saturated ammonium chloride solution
  3. additionThe reaction mixture was diluted with EtOAc
  4. filtrationfiltered through a Celite bed
  5. additionThe filtrate was diluted with EtOAc
  6. washthe organic layer was washed with water and brine
  7. customThe solvent was evaporated under reduced pressure
  8. customThe crude product was purified by column chromatography (silica 60-120 mesh, eluent 5% EtOAc in petroleum ether)

출처 및 근거

ORD 기록
ord-c200f8db42a84c4b8bd7b7787641c199
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901156B2

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