p-Toluenesulfonic acid → cis-4-Tetrahydropyranyloxy 2-cyclopentenol

HRID 1855944

反応式

HRID 1855944 の反応式
[CH:1]1([OH:7])[CH2:5][CH:4]([OH:6])[CH:3]=[CH:2]1.C1(C)C=CC(S(O)(=O)=O)=CC=1.[O:19]1[CH:24]=[CH:23][CH2:22][CH2:21][CH2:20]1>C(Cl)Cl.N1C=CC=CC=1.O1CCCC1>[O:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[O:6][C@@H:4]1[CH2:5][C@H:1]([OH:7])[CH:2]=[CH:3]1

参加物

7

反応物 3

HCID 6101p-Toluenesulfonic acidHCID 80803,4-dihydro-2H-pyranHCID 2786004-Cyclopentene-1,3-diol

生成物 1

HCID 13623252cis-4-Tetrahydropyranyloxy 2-cyclopentenol収率 71.7%

試薬・触媒・溶媒 3

HCID 1049Pyridine触媒HCID 8028Tetrahydrofuran触媒HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of 5.0 g of 2-cyclopentene-1,4-diol in 300 ml of methylene chloride was added 5 ml of a solution of p-toluenesulfonic acid in tetrahydrofuran (1 millimole/100 ml). A solution of 4.2 g of 2,3-dihydropyran in 30 ml of methylene chloride was then added dropwise with stirring over a period of 1 hour. After stirring overnight at room temperature, 8 drops of pyridine were added. The methylene chloride was evaporated and the residue was dissolved in diethyl ether, washed with water and dried. The residual obtained by evaporating the solvent was chromatographed on silica gel (200 g) using chloroform as an eluent. First, the diether product flowed out. The subsequent effluent was treated in a customary manner to afford 6.6 g of cis-4-tetrahydropyranyloxy 2-cyclopentenol as colorless oily substance boiling at 84° C. (0.7 mmHg).

後処理

  1. stirringAfter stirring overnight at room temperature
  2. customThe methylene chloride was evaporated
  3. dissolutionthe residue was dissolved in diethyl ether
  4. washwashed with water
  5. customdried
  6. customThe residual obtained
  7. customby evaporating the solvent
  8. customwas chromatographed on silica gel (200 g)
  9. additionThe subsequent effluent was treated in a customary manner

出典と根拠

ORDレコード
ord-607412bea2924885b7a1a436db1424ca
出典データセット
uspto-grants-1980_08
特許番号
US04217284

関連ノート

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