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3,4-dihydro-2H-pyran → 2-[(2-Bromophenyl)methoxy]oxane

HRID 428004
ノート
印刷プレビュー

反応式

HRID 428004 の反応式
[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][OH:5].[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH2:11]1.C(=O)(O)[O-].[Na+]>C(Cl)Cl.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][O:5][CH:11]1[CH2:12][CH2:13][CH2:14][CH2:15][O:10]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 80803,4-dihydro-2H-pyranHCID 728502-Bromobenzyl alcoholHCID 516892Sodium Bicarbonate

生成物 1

HCID 53150262-[(2-Bromophenyl)methoxy]oxane収率 99.3%

試薬・触媒・溶媒 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)触媒HCID 6344
Dichloromethane
溶媒

実験手順

Pyridinium p-toluenesulfonate (0.30 g) was added to a solution of 2-bromobenzylalcohol (25.00 g, 0.134 mol) in methylene chloride (100 ml), and the mixture was stirred at room temperature. 3,4-Dihydro-2H-pyran (16.86 g, 0.200 mol) was added thereto. The mixture was stirred at room temperature for 2 hours, and saturated aqueous sodium bicarbonate solution (200 ml) was added. The resulting mixture was extracted with methylene chloride and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave the desired compound 1-bromo-2-(tetrahydropyran-2-yloxymethyl)benzene (36.00 g, 99.3%) as an oil.

後処理

  1. stirringThe mixture was stirred at room temperature for 2 hours
  2. extractionThe resulting mixture was extracted with methylene chloride
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customEvaporation of the solvent

出典と根拠

ORDレコード
ord-3f4c753e6db9454fb6153bf8bb0fb11b
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313150B1

反応ノート

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