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Acetamide, 2-bromo-N-butyl-N-methyl- → 2-(acetylthio)-N-butyl-N-methylacetamide

HRID 1006766
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인쇄 미리보기

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HRID 1006766 반응식
Br[CH2:2][C:3]([N:5]([CH2:7][CH2:8][CH2:9][CH3:10])[CH3:6])=[O:4].[C:11]([O-:14])(=[S:13])[CH3:12].[K+]>CO>[C:11]([S:13][CH2:2][C:3]([N:5]([CH2:7][CH2:8][CH2:9][CH3:10])[CH3:6])=[O:4])(=[O:14])[CH3:12]
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참가 물질

4

반응물 2

HCID 10798390Acetamide, 2-bromo-N-butyl-N-methyl-HCID 23670855Potassium ethanethioate

생성물 1

HCID 197086942-(acetylthio)-N-butyl-N-methylacetamide수율 100%

시약·촉매·용매 1

HCID 887Methanol용매2회

반응 조건

온도
40 °C

실험 절차

4.16 g of bromo-N-butyl-N-methylacetamide of Preparation B of Example 78, Step A in 1.5 ml of methanol were added to a suspension of 2.28 g of potassium thioacetate in 10 ml of methanol and the mixture was heated for one hour at 40° C. under an argon atmosphere. After evaporation to dryness under reduced pressure, the residue was dissolved with ethyl ether, the insoluble part filtered off and the solution was evaporated to dryness to obtain 4.06 g of oily product.

후처리

  1. customAfter evaporation to dryness under reduced pressure
  2. dissolutionthe residue was dissolved with ethyl ether
  3. filtrationthe insoluble part filtered off
  4. customthe solution was evaporated to dryness

출처 및 근거

ORD 기록
ord-686997355a1c4c90be147b7716837c98
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06790971B1

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