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Sodium Carbonate → (3-Ethyl-2-pentenyl)-phenylsulfone

HRID 1706052
ノート
印刷プレビュー

反応式

HRID 1706052 の反応式
C(=O)([O-])[O-].[Na+].[Na+].[C:7]1([S:13]([O-:15])=[O:14])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[Na+].Br[CH2:18][CH:19]=[C:20]([CH2:23][CH3:24])[CH2:21][CH3:22]>CO>[CH2:21]([C:20]([CH2:23][CH3:24])=[CH:19][CH2:18][S:13]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:15])=[O:14])[CH3:22]
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 3

HCID 10340Sodium CarbonateHCID 2723840Benzenesulfinic acid, sodium saltHCID 109650661-bromo-3-ethyl-2-pentene

生成物 1

HCID 20336764(3-Ethyl-2-pentenyl)-phenylsulfone収率 80.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

1.85 gm of sodium carbonate and 18.5 gm of sodium phenyl sulfinate were introduced into 60 cc of methanol. Then 20 gm of 1-bromo-3-ethyl-2-pentene were added within the space of about 30 minutes at room temperature to the resulting suspension, which then was agitated for 1 hour and 30 minutes at room temperature. Then the reaction mixture was poured into ice-water and the organic phase was was separated by decanting. The aqueous phase was extracted with ethyl ether and the ether extracts were combined with the principal organic solution. The solution thus obtained was dried over magnesium sulfate and the solvent was removed under reduced pressure to obtain 21.665 gm of (3-ethyl-2-pentenyl)-phenylsulfone. A sample of this product was rectified under reduced pressure and the boiling point was 125° C. under 0.02 mm pressure of mercury and its refractive index nD23 =1.530.

後処理

  1. customthe organic phase was was separated
  2. customby decanting
  3. extractionThe aqueous phase was extracted with ethyl ether
  4. customThe solution thus obtained
  5. dry with materialwas dried over magnesium sulfate
  6. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-25fd3dca2e1342d4a22b6f3f92b7786c
出典データセット
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04206140

反応ノート

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