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Hydrochloric Acid → Methyl 4-cyano-3-oxobutanoate

HRID 1837319
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HRID 1837319 반응식
[C-:1]#[N:2].[K+].Br[CH2:5][C:6](=[O:12])[CH2:7][C:8]([O:10][CH3:11])=[O:9].Cl>CO>[C:1]([CH2:5][C:6](=[O:12])[CH2:7][C:8]([O:10][CH3:11])=[O:9])#[N:2]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 9032Potassium CyanideHCID 295655Methyl 4-bromo-3-oxobutanoate2회

생성물 1

HCID 9964118Methyl 4-cyano-3-oxobutanoate수율 85.3%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

10.0 g of potassium cyanide was dissolved in 400 ml of methanol, to which then 24.8 g of methyl 4-bromo-3-oxobutanoate was added dropwise from a dropping funnel over 20 minutes. Methyl 4-bromo-3-oxobutanoate remaining in the dripping funnel was dissolved further in 10 ml of methanol and added dropwise, and the mixture was stirred with cooling on ice for 1 hour and at room temperature for 2 hours. Subsequently, the reaction mixture was cooled on ice, and treated dropwise with 3 ml of a concentrated hydrochloric acid. The reaction mixture was extracted three times with diethylether (2000 ml of diethylether in total). The organic layers were combined, washed twice with 100 ml of saturated brine, dried over magnesium sulfate, concentrated under reduced pressure to obtain 15.3 g of methyl 4-cyano-3-oxobutanoate (purity: 83%).

후처리

  1. additionadded dropwise
  2. temperatureSubsequently, the reaction mixture was cooled on ice
  3. extractionThe reaction mixture was extracted three times with diethylether (2000 ml of diethylether in total)
  4. washwashed twice with 100 ml of saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-de631344d32c4461a0703e529e3df0eb
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06781009B2

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