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Thionyl Chloride → 1-Chloro-2-methyl-6-phenoxy-hexane

HRID 2083106
ノート
印刷プレビュー

反応式

HRID 2083106 の反応式
S(Cl)([Cl:3])=O.O[CH2:6][CH:7]([CH3:19])[CH2:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(Cl)(Cl)Cl.CN(C=O)C>[Cl:3][CH2:6][CH:7]([CH3:19])[CH2:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
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 2

HCID 24386Thionyl ChlorideHCID 203221341-Hydroxy-2-methyl-6-phenoxyhexane

生成物 1

HCID 203221511-Chloro-2-methyl-6-phenoxy-hexane

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒2 回HCID 6228Dimethylformamide溶媒

実験手順

A solution of 60 g of thionyl chloride in 50 ml of CHCl3 was added dropwise to 100 g of 1-Hydroxy-2-methyl-6-phenoxyhexane in 200 ml of CHCl3 and 0.5 ml of DMF. The solution was refluxed until the development of the gas was finished and then poured onto ice. The aqueous phase was extracted twice with CHCl3 and the combined organic phases were washed with water and finally with a saturated NaHCO3 -solution, dried with MgSO4, evaporated and the residue was distilled off. Boiling point0.5 : 117° - 120° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureThe solution was refluxed until the development of the gas
  2. additionpoured onto ice
  3. extractionThe aqueous phase was extracted twice with CHCl3
  4. washthe combined organic phases were washed with water and finally with a saturated NaHCO3 -solution
  5. dry with materialdried with MgSO4
  6. customevaporated
  7. distillationthe residue was distilled off
  8. custom117° - 120° C.

出典と根拠

ORDレコード
ord-8f7b55bb3ecb4d3ba29fd66b34a5ecf5
出典データセット
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04083990

反応ノート

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