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Propargyl bromide → 4-Fluoro-N-(prop-2-yn-1-yl)aniline

HRID 1722705
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HRID 1722705 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=1.Br[CH2:10][C:11]#[CH:12].C(N(C(C)C)C(C)C)C.C(OCC)(=O)C>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:12][C:11]#[CH:10])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7842Propargyl bromideHCID 8857Ethyl AcetateHCID 97314-FluoroanilineHCID 81531Diisopropylethylamine

생성물 1

HCID 146500364-Fluoro-N-(prop-2-yn-1-yl)aniline

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A solution of 9.47 ml (0.1 mol) of 4-fluorobenzenamine, 16.36 g (0.11 mol) of an 80% solution of 3-bromo-1-propyne in toluene, and 17.43 ml (0.11 mol) of N-ethyl-N-(1-methylethyl)-2-propanamine in 350 ml of toluene is heated at 90° C. for three hours. Ethyl acetate is added to the reaction suspension, and it is washed three times with water. The organic layer is separated, dried (magnesium sulfate), and concentrated to give 15.5 g of a dark brown liquid. This is applied to a column of 1 kg of flash silica gel packed in heptane-dichloromethane (5:1). Elution with the same solvent gives 9.09 g (61%) of the product as a yellow oil.

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후처리

  1. washis washed three times with water
  2. customThe organic layer is separated
  3. dry with materialdried (magnesium sulfate)
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f767ab45708a4eb6b03112c05d2a8208
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04857530

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