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Bromopinacolone → 3-(3,3-Dimethyl-2-oxobutyl)-2.4.5-trimethylthiazol-3-ium bromide

HRID 448088
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인쇄 미리보기

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HRID 448088 반응식
[CH3:1][C:2]1[S:3][C:4]([CH3:8])=[C:5]([CH3:7])[N:6]=1.[Br:9][CH2:10][C:11](=[O:16])[C:12]([CH3:15])([CH3:14])[CH3:13]>C(#N)C>[Br-:9].[CH3:13][C:12]([CH3:15])([CH3:14])[C:11](=[O:16])[CH2:10][N+:6]1[C:5]([CH3:7])=[C:4]([CH3:8])[S:3][C:2]=1[CH3:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21642BromopinacoloneHCID 616532,4,5-Trimethylthiazole

생성물 1

HCID 866237583-(3,3-Dimethyl-2-oxobutyl)-2.4.5-trimethylthiazol-3-ium bromide수율 91.4%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
60 °C

실험 절차

A mixture of 2,4,5-trimethylthiazole (640 mg, 5 mmol) and 1-bromo-3,3-dimethylbutan-2-one (1.8 g, 10 mmol) in anhydrous acetonitrile (20 mL) was stirred at 60° C. for 5 h. The mixture was then concentrated under reduced pressure, the residue was triturated with anhydrous ethyl ether and the solid was filtered and dried under reduced pressure to provide 1.4 g of the crude title compound.

후처리

  1. concentrationThe mixture was then concentrated under reduced pressure
  2. customthe residue was triturated with anhydrous ethyl ether
  3. filtrationthe solid was filtered
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-a7abddcb3d8d4a3caae50e5c40e12f68
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481574B2

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