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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → [5-({[(1,1-Dimethylethyl)(diphenyl)silyl]oxy}methyl)-1-methyl-1h-[1,2,3]triazol-4-yl]methanol

HRID 2183517
ノート
印刷プレビュー

反応式

HRID 2183517 の反応式
C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.CC([Si](C)(C)[O:23][CH2:24][C:25]1[N:26]=[N:27][N:28]([CH3:49])[C:29]=1[CH2:30][O:31][Si:32]([C:45]([CH3:48])([CH3:47])[CH3:46])([C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)(C)C>CCO>[CH3:48][C:45]([Si:32]([C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[O:31][CH2:30][C:29]1[N:28]([CH3:49])[N:27]=[N:26][C:25]=1[CH2:24][OH:23])([CH3:46])[CH3:47]
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 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 224731964-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)-5-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)-1-methyl-1h-1,2,3-triazole

生成物 1

HCID 69793338[5-({[(1,1-Dimethylethyl)(diphenyl)silyl]oxy}methyl)-1-methyl-1h-[1,2,3]triazol-4-yl]methanol収率 89%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
50 °C

実験手順

Pyridinium para-toluenesulfonate (0.99 g, 3.94 mmol) was added to a stirred solution of 4-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-5-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)-1-methyl-1H-1,2,3-triazole (1.77 g, 3.56 mmol) in EtOH (50 ml) and then heated at 50° C. for 6 h. The reaction mixture was concentrated under reduced pressure, then taken up in EtOAc (100 ml) and washed with H2O (100 ml), 2N NaOH (100 ml) and brine (100 ml). After drying, the solvents were removed under reduced pressure and the mixture was purified by column chromatography on silica using 10-100% Et2O/iso-hexanes as eluent to yield the desired hydroxymethyltriazole (1.20 g, 89%). 1H NMR (360 MHz, CDCl3) δ 7.68-7.60 (41H, m), 7.50-7.34 (6H, m), 4.78 (2H, s), 4.46 (2H, s), 4.02 (3H, s), 1.04 (9H, s). m/z (ES+) 382 (M+H+).

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. washwashed with H2O (100 ml), 2N NaOH (100 ml) and brine (100 ml)
  3. customAfter drying
  4. customthe solvents were removed under reduced pressure
  5. customthe mixture was purified by column chromatography on silica using 10-100% Et2O/iso-hexanes as eluent

出典と根拠

ORDレコード
ord-50745dcc918343f694975f3faa25ff80
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06900209B2

反応ノート

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