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Imidazole → 3-(Tert-butyldimethylsilyloxymethyl)aniline

HRID 2235520
ノート
印刷プレビュー

反応式

HRID 2235520 の反応式
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6].N1C=CN=C1.[Si:15](Cl)([C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:17])[CH3:16].O>CN(C=O)C>[Si:15]([O:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6])([C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:17])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 795ImidazoleHCID 962WaterHCID 28928tert-Butyldimethylsilyl chlorideHCID 802933-Aminobenzyl alcohol

生成物 1

HCID 105859773-(Tert-butyldimethylsilyloxymethyl)aniline収率 62.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To 1.00 g (8.1 mmol) of 3-hydroxymethylaniline in 25 mL of DMF was added 0.61 g (8.9 mmol) of imidazole and 1.35 g (8.9 mmol) of tert-butyldimethylsilyl chloride. The reaction was stirred at room temperature for 18 h and poured into 12 volumes of water. The product was extracted with ether and the combined organic layers were washed successively with water and brine, dried over sodium sulfate, filtered and concentrated to a golden oil. The oil was purified by flash chromatography eluting with a 20% ethyl acetate/hexanes mixture to give 1.2 g (62%) of the title compound as a colorless oil.

後処理

  1. extractionThe product was extracted with ether
  2. washthe combined organic layers were washed successively with water and brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated to a golden oil
  6. customThe oil was purified by flash chromatography
  7. washeluting with a 20% ethyl acetate/hexanes mixture

出典と根拠

ORDレコード
ord-d60200cf16e44e9dba486b1f40d236c8
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07714009B2

反応ノート

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