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Hydrochloric Acid → 3-(3,4-Dimethoxyphenyl)propanenitrile

HRID 1624856
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HRID 1624856 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5](/[CH:11]=[CH:12]/[C:13]#[N:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[BH4-].[Na+].Cl>N1C=CC=CC=1.CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][C:13]#[N:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 15509583-(3,4-Dimethoxyphenyl)acrylonitrileHCID 4311764Sodium borohydride

생성물 1

HCID 3199323-(3,4-Dimethoxyphenyl)propanenitrile수율 82%

시약·촉매·용매 2

HCID 887Methanol용매HCID 1049Pyridine용매

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온도
100 °C

실험 절차

To a solution of 1 g (5.3 mmoles) of (2E)-3-(3,4-dimethoxyphenyl)prop-2-enenitrile in 9.3 mL of pyridine and 2.8 mL of methanol there is added, little by little, 0.24 g of NaBH4 (6.3 mmol, 1.2 eq.). The reaction mixture is heated at reflux (100° C.) for 9 hours. After cooling to ambient temperature, the reaction mixture is added to a solution of 9 mL of hydrochloric acid 37% in 24 g of ice. The solution is extracted twice with dichloromethane. The organic phases are collected and the solvent is evaporated off under reduced pressure to yield 0.82 g of a red-brown oil which crystallises.

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureAfter cooling to ambient temperature
  3. extractionThe solution is extracted twice with dichloromethane
  4. customThe organic phases are collected
  5. customthe solvent is evaporated off under reduced pressure

출처 및 근거

ORD 기록
ord-2b7a03b3307443438c5fe868adeec14b
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08779121B2

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