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Hydrochloric Acid → 3-Isopropyl-4-methoxyphenylacetonitrile

HRID 2076652
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HRID 2076652 반응식
[CH:1]([Mg]Br)([CH3:3])[CH3:2].Br[C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][C:15]=1[O:16][CH3:17])[CH2:10][C:11]#[N:12].Cl>O1CCCC1.[Br-].[Zn+2].[Br-]>[CH:1]([C:7]1[CH:8]=[C:9]([CH2:10][C:11]#[N:12])[CH:13]=[CH:14][C:15]=1[O:16][CH3:17])([CH3:3])[CH3:2]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 5226553-Bromo-4-methoxyphenylacetonitrileHCID 178418365HCID 178418365, 화합물

생성물 1

HCID 109103103-Isopropyl-4-methoxyphenylacetonitrile수율 83.5%

시약·촉매·용매 2

HCID 10421208Zinc bromide촉매HCID 8028Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

An isopropylmagnesium bromide-0.63M tetrahydrofuran solution (3.2 ml, 2.0 mmol) was added dropwise to a solution of zinc bromide (473 mg, 2.1 mmol) in tetrahydrofuran (2 ml) under ice-cooling. After the mixture was stirred for 15 minutes, the reaction mixture was cooled to −78° C. After 3-bromo-4-methoxybenzyl cyanide (226 mg, 1.0 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct (32 mg, 0.04 mmol) were added to the mixture at −78° C., the temperature of the reaction mixture was raised to room temperature and the mixture was further stirred for 5 hours. 1N Hydrochloric acid was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the solvent under reduced pressure was subjected to silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=8/1-6/1) to give crude (3-isopropyl-4-methoxyphenyl)acetonitrile (158 mg).

후처리

  1. temperaturecooling
  2. temperaturethe temperature of the reaction mixture was raised to room temperature
  3. stirringthe mixture was further stirred for 5 hours
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was successively washed with water
  6. dry with materiala saturated aqueous NaCl solution and dried with anhydrous sodium sulfate
  7. customThe residue obtained
  8. customby removing the solvent under reduced pressure
  9. washwas subjected to silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=8/1-6/1)

출처 및 근거

ORD 기록
ord-5878e995c9cd44a3ac082cdb4fe373ac
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07923573B2

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