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Methyl iodide → HCID 18945162、化合物

HRID 399826
ノート
印刷プレビュー

反応式

HRID 399826 の反応式
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[C:11]([N:13]2[CH:17]=[CH:16][CH:15]=[CH:14]2)[CH:12]=1)[C:6]([O:8][CH3:9])=[O:7].I[CH3:19]>C(Cl)(Cl)Cl.[Ag-]=O>[CH3:19][O:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[C:11]([N:13]2[CH:17]=[CH:16][CH:15]=[CH:14]2)[CH:12]=1)[C:6]([O:8][CH3:9])=[O:7]
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

5

反応物 2

HCID 6328Methyl iodideHCID 18945167HCID 18945167、化合物

生成物 1

HCID 18945162HCID 18945162、化合物

試薬・触媒・溶媒 2

HCID 178418778HCID 178418778、化合物触媒HCID 6212Chloroform溶媒

反応条件

温度
50 °C

実験手順

To a solution of methyl 3-hydroxymethyl-5-(pyrrol-1-yl)benzoate (2.0 g) in chloroform (30 ml) was added silver(I) oxide (8.0 g) and iodomethane (4.3 ml). The reaction mixture was stirred at 50° C. for 4.5 hours. After being cooled to room temperature, the slurry was filtered and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with a mixture of hexane and ethyl acetate (10:1). The eluted fractions containing the desired product were collected and evaporated in vacuo to afford methyl 3-methoxymethyl-5-(pyrrol-1-yl)benzoate (1.72 g)) as an oil.

後処理

  1. temperatureAfter being cooled to room temperature
  2. filtrationthe slurry was filtered
  3. customthe filtrate was evaporated in vacuo
  4. customThe residue was purified by column chromatography on silica gel eluting with a mixture of hexane and ethyl acetate (10:1)
  5. additionThe eluted fractions containing the desired product
  6. customwere collected
  7. customevaporated in vacuo

出典と根拠

ORDレコード
ord-bd68e95762104c75ac6e7228b5c4ac65
出典データセット
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05824691

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート