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Propargyl bromide → Benzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)-

HRID 1722706
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HRID 1722706 반응식
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[CH:6][CH:5]=1.Br[CH2:14][C:15]#[CH:16].C(N(C(C)C)C(C)C)C.C(OCC)(=O)C>C1(C)C=CC=CC=1.CCCCCCC.ClCCl>[CH2:16]([NH:10][C:7]1[CH:6]=[CH:5][C:4]([O:3][C:2]([F:11])([F:12])[F:1])=[CH:9][CH:8]=1)[C:15]#[CH:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 7842Propargyl bromideHCID 8857Ethyl AcetateHCID 81531DiisopropylethylamineHCID 6008484-(Trifluoromethoxy)aniline

생성물 1

HCID 14650037Benzenamine, N-2-propyn-1-yl-4-(trifluoromethoxy)-수율 66.2%

시약·촉매·용매 2

HCID 1140Toluene용매2회
HCID 21907733Dichloromethane heptane용매

실험 절차

A solution of 8.86 g (50 mmol) of 4-(trifluoromethoxy)benzenamine, 8.18 g (55 mmol) of an 80% solution of 3-bromo-1-propyne in toluene, and 8.72 ml (50 mmol) of N-ethyl-N-(1-methylethyl)-2-propanamine in 200 ml of toluene is heated at 90° C. for eighteen hours. The suspension is cooled and treated with ethyl acetate. The suspension is washed several times with water. The ethyl acetate layer is separated, dried (magnesium sulfate), and concentrated to give a brown liquid. This is applied to a column of 1 kg of flash silica gel packed in n-heptane-dichloromethane (2:1). Elution with the same solvent gives 7.12 g (66.2%) of the product as a brown liquid.

후처리

  1. temperatureThe suspension is cooled
  2. washThe suspension is washed several times with water
  3. customThe ethyl acetate layer is separated
  4. dry with materialdried (magnesium sulfate)
  5. concentrationconcentrated
  6. customto give a brown liquid
  7. washElution with the same solvent

출처 및 근거

ORD 기록
ord-97384ccf920e42868cb46dba25b9d8f7
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04857530

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