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Propargyl bromide → HCID 20565046, 화합물

HRID 126695
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HRID 126695 반응식
[Mg].Br[CH:3](Br)[CH3:4].[CH2:6](Br)C#C.[CH2:10]=[C:11]([CH2:15][CH2:16][CH3:17])[C:12](=[O:14])[CH3:13].[Cl-].[NH4+]>CCOCC>[OH:14][C:12]([CH3:6])([C:11](=[CH2:10])[CH2:15][CH2:16][CH3:17])[CH2:13][C:3]#[CH:4]
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참가 물질

7

반응물 5

HCID 7842Propargyl bromide2회HCID 112011,1-DibromoethaneHCID 25517Ammonium ChlorideHCID 5462224MagnesiumHCID 122885673-Propyl-3-buten-2-one

생성물 1

HCID 20565046HCID 20565046, 화합물

시약·촉매·용매 1

HCID 3283
Diethyl Ether
용매
3회

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온도
0 °C

실험 절차

To a mixture of 5.0 g. of magnesium and 100 mg. of mercuric chloride in 10 ml. of ether is added with stirring, one ml. of dibromoethane. The mixture is stirred for 10 minutes and 0.5 ml. of propargyl bromide is added. An additional 50 ml. of ether is added, followed by a solution of 17.5 g. of 3-methylene-2-hexanone and 27.8 g. of propargyl bromide in 60 ml. of ether, dropwise at a rate to maintain vigorous reflux. The mixture is refluxed for 1/2 hour, cooled at 0° C. and saturated ammonium chloride solution is added dropwise. The mixture is filtered through Celite and the solids are washed with ether. The ether solution is dried over magnesium sulfate and the ether is removed giving the desired product.

후처리

  1. additionTo a mixture of 5.0 g
  2. stirringThe mixture is stirred for 10 minutes
  3. temperatureThe mixture is refluxed for 1/2 hour
  4. filtrationThe mixture is filtered through Celite
  5. washthe solids are washed with ether
  6. dry with materialThe ether solution is dried over magnesium sulfate
  7. customthe ether is removed

출처 및 근거

ORD 기록
ord-a79d321e0a0b4695810e89feb9908ed6
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04254036

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