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1,4-Butanediol → 4-(Tetrahydro-2H-pyran-2-yloxy)-1-butanol

HRID 1271247
ノート
印刷プレビュー

反応式

HRID 1271247 の反応式
[CH2:1]([OH:6])[CH2:2][CH2:3][CH2:4][OH:5].[O:7]1[CH:12]=[CH:11][CH2:10][CH2:9][CH2:8]1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>ClCCl.O1CCCC1>[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:6]
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 80641,4-ButanediolHCID 80803,4-dihydro-2H-pyranHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)

生成物 1

HCID 5591134-(Tetrahydro-2H-pyran-2-yloxy)-1-butanol

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

To a solution of 100.0 g of 1,4-butanediol and 20 ml of 3,4-dihydro-2H-pyrane in 80 ml of dichloromethane and 140 ml of tetrahydrofuran, 1.8 g of pyridinium p-toluenesulfonate was added. After stirring at room temperature for 18 hours, the solvent was evaporated under reduced pressure. The residue was extracted three times with diethyl ether after adding saturated brine. After the extract was washed with a small amount of water and dried over anhydrous magnesium sulfate, the solvent was evaporated to obtain 35.98 g of the desired crude product as a colorless oily substance.

後処理

  1. customthe solvent was evaporated under reduced pressure
  2. extractionThe residue was extracted three times with diethyl ether
  3. additionafter adding saturated brine
  4. washAfter the extract was washed with a small amount of water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-44b9cf5e8c6e40888a85d7303687e717
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07205302B2

反応ノート

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