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8-Oxabicyclo[5.1.0]octan-2-one → 3-Hydroxycycloheptanone

HRID 1758163
ノート
印刷プレビュー

反応式

HRID 1758163 の反応式
[CH:1]12[O:8][CH:7]1[CH2:6][CH2:5][CH2:4][CH2:3][C:2]2=[O:9]>O1CCCC1>[OH:9][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][C:7](=[O:8])[CH2:1]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 156197338-Oxabicyclo[5.1.0]octan-2-one

生成物 1

HCID 109755023-Hydroxycycloheptanone収率 97%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a 25° C. solution of 45.9 g. (0.364 mole) of 8-oxabicyclo[5.1.0]octan-2-one in 950 ml. of 10% aqueous tetrahydrofuran was added 39.7 g. (1.47 mmoles) of aluminum amalgam. (The aluminum amalgam was prepared by 15-30 second successive washing of small pieces of aluminum foil with 2 N sodium hydroxide, distilled water, 0.5% mercuric chloride, distilled water, 2 N sodium hydroxide, distilled water, 0.5% mercuric chloride, distilled water, ethanol and ether). The mixture was stirred for 2 hours, then filtered through diatomaceous earth. The filtrate was evaporated on a rotovapor, the residue saturated with solid sodium chloride and extracted with three 500 ml. portions of ether. The ether extract was dried over magnesium sulfate and evaporated to yield 45 g. (97%) of the title compound as an oil.

後処理

  1. customTo a 25° C.
  2. washsuccessive washing of small pieces of aluminum foil with 2 N sodium hydroxide
  3. distillationdistilled water, 0.5% mercuric chloride
  4. distillationdistilled water, 2 N sodium hydroxide
  5. distillationdistilled water, 0.5% mercuric chloride
  6. distillationdistilled water, ethanol and ether)
  7. filtrationfiltered through diatomaceous earth
  8. customThe filtrate was evaporated on a rotovapor
  9. extractionthe residue saturated with solid sodium chloride and extracted with three 500 ml
  10. extractionThe ether extract
  11. dry with materialwas dried over magnesium sulfate
  12. customevaporated
  13. customto yield 45 g

出典と根拠

ORDレコード
ord-11e6f0cf1cc548b4ab6f471ea6c62986
出典データセット
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04371720

反応ノート

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