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Methanol → methyl 4-iodo-1H-pyrrole-2-carboxylate

HRID 646239
ノート
印刷プレビュー

反応式

HRID 646239 の反応式
[Na].ClC(Cl)(Cl)[C:4]([C:6]1[NH:7][CH:8]=[C:9]([I:11])[CH:10]=1)=[O:5].[CH3:14][OH:15]>>[CH3:14][O:15][C:4]([C:6]1[NH:7][CH:8]=[C:9]([I:11])[CH:10]=1)=[O:5]
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 3

HCID 887MethanolHCID 5360545Sodium2 回HCID 116816022,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)ethan-1-one

生成物 1

HCID 11673249methyl 4-iodo-1H-pyrrole-2-carboxylate収率 95%

反応条件

温度
0 °C

実験手順

To a solution of 300 mL of dry methanol was added 0.52 gm (0.023 mol) of sodium and the solution was stirred until all sodium was reacted. The solution was cooled to 0° C. and 19.5 gm (0.057 mol) of 2,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)-ethanone was added as a solid over a 15 min period. After 15 min at 0° C. the solution was warmed to room temperature and stirred for an additional 2 h. The solvents were removed at reduced pressure and the residue dissolved in diethyl ether. The ether layer was washed with H2O, saturated brine, dried (Na2SO4) and the solvents removed at reduced pressure. The solid was recystallized from hot hexanes-trace EtOAc to yield 13.7 gm (95% yield) of a light brown solid. This was used without further purification.

後処理

  1. customwas reacted
  2. temperatureAfter 15 min at 0° C. the solution was warmed to room temperature
  3. customThe solvents were removed at reduced pressure
  4. dissolutionthe residue dissolved in diethyl ether
  5. washThe ether layer was washed with H2O, saturated brine
  6. dry with materialdried (Na2SO4)
  7. customthe solvents removed at reduced pressure

出典と根拠

ORDレコード
ord-aef8f60c8e1f4d929d4dacf9cf4c210c
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07705030B2

反応ノート

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