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Diethyl Ether → alpha,alpha-Diethyl-4-methyl-3-cyclohexene-1-methanol

HRID 1719837
ノート
印刷プレビュー

反応式

HRID 1719837 の反応式
[Mg].I[CH2:3][CH3:4].[CH3:5][C:6]1[CH2:11][CH2:10][CH:9]([C:12]([OH:14])=O)[CH2:8][CH:7]=1.[CH2:15](OCC)[CH3:16]>>[CH2:15]([C:12]([CH2:3][CH3:4])([CH:9]1[CH2:10][CH2:11][C:6]([CH3:5])=[CH:7][CH2:8]1)[OH:14])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 3283Diethyl Ether2 回HCID 6340IodoethaneHCID 203504-Methyl-3-cyclohexene-1-carboxylic AcidHCID 5462224Magnesium

生成物 1

HCID 13534004alpha,alpha-Diethyl-4-methyl-3-cyclohexene-1-methanol

実験手順

To 9.4 g of magnesium stirred in 350 ml of diethyl ether was added 60.4 g of iodoethane over 30 minutes to produce a mildly refluxing reaction mixture. The reaction mixture was refluxed for an additional hour, and then 23 g of the methyl ester of 4-methyl-3-cyclohexene-1-carboxylic acid in 20 ml of diethyl ether was added dropwise while maintaining gentle reflux. The reaction mixture was refluxed for an additional 1/2 hour, quenched with water, and extracted with diethyl ether; the ether extract was washed with saturated NaCl solution, dried (MgSO4), and stripped to yield an oil, which upon distillation gave 23.2 g of product, b.p. 90° C. (1 mm).

後処理

  1. customto produce
  2. temperaturea mildly refluxing
  3. customreaction mixture
  4. temperatureThe reaction mixture was refluxed for an additional hour
  5. temperaturewhile maintaining gentle reflux
  6. temperatureThe reaction mixture was refluxed for an additional 1/2 hour
  7. customquenched with water
  8. extractionextracted with diethyl ether
  9. extractionthe ether extract
  10. washwas washed with saturated NaCl solution
  11. dry with materialdried (MgSO4)
  12. customto yield an oil, which
  13. distillationupon distillation

出典と根拠

ORDレコード
ord-f83ee87499804d35b624dd8a068e90f4
出典データセット
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04542244

反応ノート

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