Hydrochloric Acid → 3-(4-Bromophenyl)-1-dimethylamino-3-phenylthio-2-propene

HRID 1789102ノート

反応式

HRID 1789102 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH:9]=[CH:10][N:11]([CH3:13])[CH3:12])=[CH:4][CH:3]=1.P(Cl)(Cl)(Cl)=O.[C:20]1([SH:26])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C([BH3-])#N.[Na+].[OH-].[Na+].Cl>C(Cl)(Cl)Cl.C(O)(C)C.CCOCC>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([S:26][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:9][CH2:10][N:11]([CH3:13])[CH3:12])=[CH:4][CH:3]=1

参加物

10

反応物 6

HCID 313Hydrochloric AcidHCID 7969ThiophenolHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 6172441-(4-Bromophenyl)-3-(dimethylamino)-2-propen-1-oneHCID 5003444Sodium cyanoborohydride

生成物 1

HCID 537682463-(4-Bromophenyl)-1-dimethylamino-3-phenylthio-2-propene

試薬・触媒・溶媒 3

HCID 3283Diethyl Ether溶媒HCID 3776Isopropanol溶媒HCID 6212Chloroform溶媒

実験手順

By using a method similar to that described in Example 35, but starting from 1-(4-bromophenyl)-3-dimethylamino-2-propen-1-one (10 g), phosphorus oxychloride (3.64 g), thiophenol (4.2 cc) and sodium cyanoborohydride (1.47 g), a residue is obtained which is taken up in chloroform. The solution is adjusted to pH 10 by adding a concentrated aqueous solution of sodium hydroxide. The organic phase is separated and then the aqueous phase is extracted with methylene chloride. The organic phases are collected, dried over sodium sulphate, filtered and then evaporated to dryness under reduced pressure (2.6 kPa) at 30° C. to give a residue which is dissolved in isopropanol (30 cc). A 3N ether solution (13 cc) of hydrochloric acid gas is added to the solution obtained. The white solid which precipitates is separated off by filtration and recrystallised twice from ispropanol (40 cc). In this way 3-(4-bromophenyl)-1-dimethylamino-3-phenylthio-2-propene (E) hydrochloride (4.8 g) is obtained in the form of white crystals melting at 187° C.

後処理

  1. customa residue is obtained which
  2. customThe organic phase is separated
  3. extractionthe aqueous phase is extracted with methylene chloride
  4. customThe organic phases are collected
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. customevaporated to dryness under reduced pressure (2.6 kPa) at 30° C.
  8. customto give a residue which
  9. customobtained
  10. customThe white solid which precipitates
  11. customis separated off by filtration
  12. customrecrystallised twice from ispropanol (40 cc)

出典と根拠

ORDレコード
ord-cf43cabef56e42ff831c0043b831c695
出典データセット
uspto-grants-1987_08
特許番号
US04686309

反応ノート

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