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Iodine → 3-(3-iodo-4-methoxybenzyl)-1H-1,2,4-triazole

HRID 1508549
ノート
印刷プレビュー

反応式

HRID 1508549 の反応式
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]([CH2:7][C:8]2[N:12]=[CH:11][NH:10][N:9]=2)=[CH:5][CH:4]=1.[I:15]I>CO.S([O-])([O-])(=O)=O.[Ag+2]>[I:15][C:14]1[CH:13]=[C:6]([CH:5]=[CH:4][C:3]=1[O:2][CH3:1])[CH2:7][C:8]1[N:12]=[CH:11][NH:10][N:9]=1
参加物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 807IodineHCID 178489902HCID 178489902、化合物

生成物 1

HCID 1784899043-(3-iodo-4-methoxybenzyl)-1H-1,2,4-triazole

試薬・触媒・溶媒 2

HCID 178418844HCID 178418844、化合物触媒2 回HCID 887Methanol溶媒

実験手順

To a solution of 3-(4-methoxybenzyl)-1H-1,2,4-triazole (335 mg, 1.770 mmol) in MeOH (5 ml) under nitrogen at RT was added silver sulfate (552 mg, 1.770 mmol) followed by iodine (449 mg, 1.770 mmol). Added a second equivalent of silver sulfate and stirred for 3 days. The reaction did not go to completion. The solids were filtered washing with MeOH, the filtrate was concentrated, and the residue was purified by flash column chromatography on silica gel, eluting with MeOH in DCM to afford the title compound contaminated with ca. 20% of starting material. Mass spectrum (ESI) 316.1 (M+1).

後処理

  1. filtrationThe solids were filtered
  2. washwashing with MeOH
  3. concentrationthe filtrate was concentrated
  4. customthe residue was purified by flash column chromatography on silica gel
  5. washeluting with MeOH in DCM

出典と根拠

ORDレコード
ord-cfaa3d88e7654d019e04623a8f363db9
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221834B2

反応ノート

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