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Hydrochloric Acid → 2-(3-Formyl-2-thienyl)-4-methylbutyronitrile

HRID 1071630
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HRID 1071630 반응식
[O:1]1CCO[CH:2]1[C:6]1[CH:10]=[CH:9][S:8][C:7]=1[CH:11]([CH2:14][CH2:15][CH3:16])[C:12]#[N:13].Cl>CC(C)=O.[Cl-].[Na+].O>[CH:2]([C:6]1[CH:10]=[CH:9][S:8][C:7]=1[CH:11]([CH2:14][CH2:15][CH3:16])[C:12]#[N:13])=[O:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 223936462-[3-(1,3-Dioxolan-2-yl)-2-thienyl]-4-methylbutyronitrile

생성물 1

HCID 223935692-(3-Formyl-2-thienyl)-4-methylbutyronitrile수율 94.3%

시약·촉매·용매 2

HCID 180Acetone용매HCID 57417360Sodium chloride; water용매

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온도
70 °C
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실험 절차

2.16 g (9.10 mmol) of 2-[3-(1,3-dioxolan-2-yl)-2-thienyl]-4-methylbutyronitrile was dissolved in 40 ml of acetone, 115 ml of 5N HCl was added, and the mixture was heated at 70° C. for 3 minutes. After completion of the reaction, brine was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and evaporated, to give a crude product. The crude product was subjected to 75 g of silica gel (ethyl acetate:hexane=1:2), to give 1.66 g (8.58 mmol, 94.3%) of the title compound as a brown oil.

후처리

  1. additionwas added
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customto give a crude product

출처 및 근거

ORD 기록
ord-7b6e4081b7b04928913534e264455d56
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06906072B1

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