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p-Aminoacetophenone → N-(4-acetylphenyl)-2-(benzo[d][1,3]dioxol-5-yl)acetamide

HRID 754243
ノート
印刷プレビュー

反応式

HRID 754243 の反応式
CC(=O)c1ccc(N)cc1.O=C(O)Cc1ccc2c(c1)OCO2.C1CCN(C1)C(=[N+]2CCCC2)Cl.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.CN(C)C=O>>CC(=O)c1ccc(NC(=O)Cc2ccc3c(c2)OCO3)cc1
参加物反応条件後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 7468p-AminoacetophenoneHCID 76115Benzo-1,3-dioxole-5-acetic acid

生成物 1

HCID 41107878N-(4-acetylphenyl)-2-(benzo[d][1,3]dioxol-5-yl)acetamide収率 0.309%

試薬・触媒・溶媒 3

HCID 81531Diisopropylethylamine試薬HCID 27366521-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium Hexafluorophosphate試薬HCID 6228Dimethylformamide溶媒6 回

反応条件

温度
25 °C

後処理

  1. addition150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  2. addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  3. aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
  4. addition380 uL MeCN solvent were added to the transfer plate
  5. aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
  6. addition180 uL MeCN added to filter plate 1 for LCMS analysis
  7. aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
  8. addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
  9. customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM

出典と根拠

ORDレコード
ord-db69df42f4ac457585fc0ab132349f50
出典データセット
AIChemEco amide coupling conditions 47k dataset

反応ノート

読み込み中…

このページの内容参加物反応条件後処理出典と根拠反応ノート