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Hydrochloric Acid → HCID 12256609、化合物

HRID 730038
ノート
印刷プレビュー

反応式

HRID 730038 の反応式
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=O)=O)=[CH:7][CH:6]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].Cl.S(OC)(O[CH3:26])(=O)=O.[OH-].[Na+]>C(OCC)C>[Cl:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:26])=[CH:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 6497Dimethyl SulfateHCID 14798Sodium HydroxideHCID 122565944-(3-Chloropropyl)benzenesulfonyl chlorideHCID 21226445Aluminium lithium hydride2 回

生成物 1

HCID 12256609HCID 12256609、化合物

試薬・触媒・溶媒 1

HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

At room temperature, a solution of 10b (12.7 g; 5.0 mmol) in diethyl ether (75 ml) was added dropwise over a period of 2.5 h to a suspension of LiAlH4 (2.9 g; 7.6 mmol) in diethyl ether (50 ml). After the addition had ended, the reaction mixture was stirred at room temperature and with occasional addition of LiAlH4 until no more starting material could be detected by thin-layer chromatography (2.5 h). With ice-cooling, ice was introduced into the reaction mixture, and the aqueous phase was acidified with 10% hydrochloric acid (pH 1). The organic phase was removed and the aqueous phase was extracted with diethyl ether (3×). The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it was virtually colorless. Dimethyl sulfate (9.0 g; 7.0 mmol) was added to the combined sodium hydroxide extract, and the mixture was stirred at room temperature for 16.5 h. The oily sediment was taken up in diethyl ether. The organic phase was separated off and the aqueous phase was again extracted with diethyl ether (2×). The combined organic extract was dried over Na2SO4 and concentrated. The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.).

後処理

  1. additionAfter the addition
  2. customcould be detected by thin-layer chromatography (2.5 h)
  3. temperatureWith ice-cooling
  4. additionice was introduced into the reaction mixture
  5. customThe organic phase was removed
  6. extractionthe aqueous phase was extracted with diethyl ether (3×)
  7. extractionThe combined organic extract
  8. washwas washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it
  9. extractionextract
  10. customThe organic phase was separated off
  11. extractionthe aqueous phase was again extracted with diethyl ether (2×)
  12. extractionThe combined organic extract
  13. dry with materialwas dried over Na2SO4
  14. concentrationconcentrated
  15. distillationThe brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.)

出典と根拠

ORDレコード
ord-7f89c731b69b43eb9f8a644e38ac892f
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07582660B2

反応ノート

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