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

HRID 1722706
ノート
印刷プレビュー

反応式

HRID 1722706 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒2 回
HCID 21907733Dichloromethane heptane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-97384ccf920e42868cb46dba25b9d8f7
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04857530

反応ノート

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