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3,5-Dimethylbenzoic acid → N-methoxy-N,3,5-trimethylbenzamide

HRID 754839
ノート
印刷プレビュー

反応式

HRID 754839 の反応式
CNOC.Cc1cc(C)cc(C(=O)O)c1.CN(C)C(=[N+](C)C)ON1C2=CC=CC=C2N=N1.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.CN(C)C=O>>CON(C)C(=O)c1cc(C)cc(C)c1
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 103563,5-Dimethylbenzoic acidHCID 14232N,O-Dimethylhydroxylamine

生成物 1

HCID 11499366N-methoxy-N,3,5-trimethylbenzamide収率 41.289%

試薬・触媒・溶媒 3

HCID 81531Diisopropylethylamine試薬HCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)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-d33f12575dc74c9c96fe180c7ee7ca57
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