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Sodium cyanoborohydride → Benzenemethanamine, 4-fluoro-N-methoxy-

HRID 1836462
ノート
印刷プレビュー

反応式

HRID 1836462 の反応式
[CH3:1][O:2][N:3]=[CH:4][C:5]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][CH:6]=1.C([BH3-])#N.[Na+]>C(O)(=O)C>[F:11][C:8]1[CH:7]=[CH:6][C:5]([CH2:4][NH:3][O:2][CH3:1])=[CH:10][CH:9]=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

4

反応物 2

HCID 5003444Sodium cyanoborohydrideHCID 539632384-Fluoro-benzaldehyde O-methyl-oxime

生成物 1

HCID 12147060Benzenemethanamine, 4-fluoro-N-methoxy-収率 75%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
25 °C

実験手順

In an alternative procedure a solution of 4-fluorobenzaldehyde O-methyloxime (0.82 g, 5.35 mmol) in acetic acid ( 8 ml ) was treated at 10° C. with sodium cyanoborohydride (0.67 g, 10.7 mmol) added in small portions over 10 min and the resulting solution was stirred at 25° C. for 18 h. The solvent was evaporated under reduced pressure (co-evaporation with toluene twice) and the residue was slurried with water and the pH was adjusted to 9 with 2 N aqueous sodium hydroxide. The aqueous phase was extracted twice with ether and the combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated under reduced pressure. The residual oil was chromatographed on silica gel (elution hexane-ethyl acetate, 8:2) and distilled in vacuo to give 0.62 g (75% yield) of the title amine as a clear oil.

後処理

  1. additionadded in small portions over 10 min
  2. customThe solvent was evaporated under reduced pressure (co-evaporation with toluene twice) and the residue
  3. extractionThe aqueous phase was extracted twice with ether
  4. washthe combined organic extracts were washed with brine
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated under reduced pressure
  7. customThe residual oil was chromatographed on silica gel (elution hexane-ethyl acetate, 8:2)
  8. distillationdistilled in vacuo

出典と根拠

ORDレコード
ord-9566c8a0c167463ea3cc97075fef2179
出典データセット
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06777440B2

反応ノート

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