Water → (+/-)-4-(4-Chlorobenzyl)-2-[(4-chloro-2-methoxyphenoxy)methyl]morpholine oxalic acid salt

HRID 1532993

反応式

HRID 1532993 の反応式
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][O:10][CH:9]([CH2:13]Cl)[CH2:8]2)=[CH:4][CH:3]=1.[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([OH:24])=[C:20]([O:25][CH3:26])[CH:19]=1.[O-]CC.[K+].C1OCCOCCOCCOCCOCCOC1.[OH2:49]>C1(C)C=CC=CC=1>[C:20]([OH:25])(=[O:10])[C:21]([OH:24])=[O:49].[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][O:10][CH:9]([CH2:13][O:24][C:21]3[CH:22]=[CH:23][C:18]([Cl:17])=[CH:19][C:20]=3[O:25][CH3:26])[CH2:8]2)=[CH:4][CH:3]=1

参加物

7

反応物 5

HCID 962WaterHCID 280504-ChloroguaiacolHCID 2855718-Crown-6HCID 11345975Morpholine, 2-(chloromethyl)-4-[(4-chlorophenyl)methyl]-HCID 23670592Potassium ethoxide

生成物 1

HCID 69687298(+/-)-4-(4-Chlorobenzyl)-2-[(4-chloro-2-methoxyphenoxy)methyl]morpholine oxalic acid salt

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of (±)-4-(4-chlorobenzyl)-2-chloromethylmorpholine (10.0 g, 38.5 mmol), 4-chloro-2-methoxyphenol (9.0 g, 58 mmol), potassium ethoxide (6.5 g, 77 mmol), and 18-crown-6 (10.2 g, 38.5) was refluxed in toluene (100 ml) for 34 h. Water (200 ml) was added and the phases were separated. Drying and evaporation of the toluene phase was followed by column chromatography on silica gel with 3% ethanol in dichloromethane as eluent. The free base was dissolved in ether and precipitated with oxalic acid to give the title compound. Yield 10.3 g, 57%, mp 133-139° C.

後処理

  1. customthe phases were separated
  2. customDrying
  3. customevaporation of the toluene phase
  4. dissolutionThe free base was dissolved in ether
  5. customprecipitated with oxalic acid

出典と根拠

ORDレコード
ord-686e92d75890400784bd55bd75a4f4e5
出典データセット
uspto-grants-2001_03
特許番号
US06207662B1

関連ノート

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