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3-Chloroaniline → 7-Chloro-4-methylquinoline

HRID 6601
ノート
印刷プレビュー

反応式

HRID 6601 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].CO[CH2:11][CH2:12][C:13](OC)(OC)[CH3:14]>[Cl-].[Zn+2].[Cl-].C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:6]([C:13]([CH3:14])=[CH:12][CH:11]=[N:5]2)=[CH:7][CH:8]=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 79323-ChloroanilineHCID 810844-Methoxybutan-2-one-dimethylacetal

生成物 1

HCID 1704377-Chloro-4-methylquinoline

試薬・触媒・溶媒 2

HCID 3007855Zincchloride触媒HCID 702Ethanol溶媒

実験手順

To a mixture containing 3-chloroaniline (1.59 g), ferric chloride hexahydrate (5.4 g), zinc chloride (0.2 g), ethanol (20 ml of 95% aqueous solution) preheated to 60° C. was added 1,3,3-trimethoxybutane (1.48 g). The resulting mixture was refluxed for two hours and allowed to stand overnight. The volatile matrials were then removed in vacuo and the residue rendered basic with 10% aqueous sodium hydroxide. The resulting mixture was partitioned between water and diethyl ether (3 times). The combined ether layer was dried over magnesium sulfate. Rotary evaporation of the ether solution gave a dark liquid. The liquid was added to a silica gel column and eluted with hexane/ethyl acetate (3:1) to give the desired product as tan crystals.

後処理

  1. custompreheated to 60° C.
  2. temperatureThe resulting mixture was refluxed for two hours
  3. customThe volatile matrials were then removed in vacuo
  4. customThe resulting mixture was partitioned between water and diethyl ether (3 times)
  5. dry with materialThe combined ether layer was dried over magnesium sulfate
  6. customRotary evaporation of the ether solution
  7. customgave a dark liquid
  8. additionThe liquid was added to a silica gel column
  9. washeluted with hexane/ethyl acetate (3:1)

出典と根拠

ORDレコード
ord-cf2f96f6b259443b9d352b9132f225ad
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07083982B2

反応ノート

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