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Methanol → 1-(4-Bromo-2-fluorophenyl)ethan-1-amine

HRID 339138
ノート
印刷プレビュー

反応式

HRID 339138 の反応式
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([F:10])[CH:3]=1.[CH3:11][Mg]Br.CO.[BH4-].[Na+]>C1COCC1.C(OCC)C>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]([NH2:7])[CH3:11])=[C:4]([F:10])[CH:3]=1
参加物反応条件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 887MethanolHCID 7360294-Bromo-2-fluorobenzonitrileHCID 4311764Sodium borohydrideHCID 178418573HCID 178418573、化合物

生成物 1

HCID 185435761-(4-Bromo-2-fluorophenyl)ethan-1-amine収率 44%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

To a solution of 12 g of 4-bromo-2-fluorobenzonitrile (60 mM) in THF (120 ml) were added 75 ml (150 mM) of a 2 M solution of methylmagnesium bromide in diethyl ether at 0° C. The reaction mixture was stirred at 0° C. for 6 h. Then 200 ml of methanol were added gradually to the reaction mixture. Subsequently, 5.7 g (150 mM) of sodium borohydride were added in portions, and the mixture was stirred at room temperature for 16 h. Thereafter, the reaction mixture was concentrated under reduced pressure, and 200 ml of water were added. The pH was adjusted to pH=˜1 with 2 M HCl, and the aqueous solution was extracted with chloroform. Subsequently, the pH was adjusted to pH=˜9 with 2M NaOH, and extraction was effected with chloroform (2×100 ml). The combined chloroform extracts were dried, and the solvent was removed under reduced pressure. 7.3 g (44%) of 1-(4-bromo-2-fluorophenyl)ethanamine were obtained as a yellow oil.

後処理

  1. stirringthe mixture was stirred at room temperature for 16 h
  2. concentrationThereafter, the reaction mixture was concentrated under reduced pressure, and 200 ml of water
  3. additionwere added
  4. extractionthe aqueous solution was extracted with chloroform
  5. extractionSubsequently, the pH was adjusted to pH=˜9 with 2M NaOH, and extraction
  6. dry with materialThe combined chloroform extracts were dried
  7. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-b6bbb2fab1e442519fd838c44c473ea1
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889878B2

反応ノート

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