Thionyl Chloride → Fluoranthene, 1-(chloromethyl)-

HRID 2255820ノート

反応式

HRID 2255820 の反応式
O[CH2:2][C:3]1[C:17]2=[C:18]3[C:10]([C:11]4[C:16]2=[CH:15][CH:14]=[CH:13][CH:12]=4)=[CH:9][CH:8]=[CH:7][C:6]3=[CH:5][CH:4]=1.O=S(Cl)[Cl:21]>C1(C)C=CC=CC=1>[Cl:21][CH2:2][C:3]1[C:17]2=[C:18]3[C:10]([C:11]4[C:16]2=[CH:15][CH:14]=[CH:13][CH:12]=4)=[CH:9][CH:8]=[CH:7][C:6]3=[CH:5][CH:4]=1

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 1544331-Hydroxymethylfluoranthene

生成物 1

HCID 152291Fluoranthene, 1-(chloromethyl)-

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

To a RB flask equipped with magnetic stirring bar, condenser, addition funnel, thermometer and N2 inlet line with bubbler was added 1-hydroxymethylfluoranthene (3B, 12.0 g, 0.052 mol), and dry PhCH3 (500 mL). To the mixture was added SOCl2 (Aldrich, 15.73 g, 0.132 mol, 9.5 mL) dropwise over 15 min. The mixture was then heated at 80° overnight and then refluxed for 1 h. The solvent was removed by rotary evaporation to give a crude off white solid. The material was redissolved in PhCH3 (300 mL) followed again by rotary evaporation. The process was repeated two additional times to give the crude product 1-chloromethylfluoranthene which was used without further purification.

後処理

  1. customTo a RB flask equipped with magnetic stirring bar, condenser, addition funnel
  2. temperatureThe mixture was then heated at 80° overnight
  3. temperaturerefluxed for 1 h
  4. customThe solvent was removed by rotary evaporation
  5. customto give a crude off white solid
  6. customfollowed again by rotary evaporation

出典と根拠

ORDレコード
ord-415362ab5d5546458b1bfed2bdfa1682
出典データセット
uspto-grants-1993_08
特許番号
US05241107

反応ノート

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