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Methylamine → 3-Benzyloxy-1-methylazetidine

HRID 328899
ノート
印刷プレビュー

反応式

HRID 328899 の反応式
[CH2:1]([O:8][CH:9]([CH2:12]Cl)[CH2:10]Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:14][NH2:15].[OH-].[Na+]>>[CH2:1]([O:8][CH:9]1[CH2:12][N:15]([CH3:14])[CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 6329MethylamineHCID 14798Sodium HydroxideHCID 5155009Benzene, [[2-chloro-1-(chloromethyl)ethoxy]methyl]-

生成物 1

HCID 205173843-Benzyloxy-1-methylazetidine収率 47%

反応条件

温度
90 °C

実験手順

21.9 parts of 2-benzyloxy-1,3-dichloro-propane and 77.5 parts of monomethylamine (40% aqueous solution) were added to an autoclave and they were heated at 90° C. for 48 hours with agitation. The reaction mixture was cooled and 120 parts of 2N-NaOH aqueous solution were added thereto. Then the mixture was heated to distill off excessive monomethylamine. The remaining liquor was extracted twice with 200 parts of ether, and the extract was washed with 100 parts of water, extracted with 100 parts of 2N-HCl aqueous solution and further extracted with 50 parts of 2N-HCl aqueous solution. The water layers were combined, washed with 50 parts of ether and made sufficiently alkaline with 2N-NaOH aqueous solution. The liquor was extracted twice with 100 parts of ether, and the ether extract was washed in 50 parts of water and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was subjected to distillation to yield 8.3 parts of 3 -benzyloxy-1-methylazetidine boiling at 80° - 82° C. The yield was 47%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the product are as follows:

後処理

  1. temperatureThe reaction mixture was cooled
  2. temperatureThen the mixture was heated
  3. distillationto distill off excessive monomethylamine
  4. extractionThe remaining liquor was extracted twice with 200 parts of ether
  5. washthe extract was washed with 100 parts of water
  6. extractionextracted with 100 parts of 2N-HCl aqueous solution
  7. extractionfurther extracted with 50 parts of 2N-HCl aqueous solution
  8. washwashed with 50 parts of ether
  9. extractionThe liquor was extracted twice with 100 parts of ether
  10. extractionthe ether extract
  11. washwas washed in 50 parts of water
  12. dry with materialdried over anhydrous sodium sulfate
  13. distillationThe solvent was distilled off
  14. distillationthe residue was subjected to distillation

出典と根拠

ORDレコード
ord-0c079c1c77164e4cbc510b6a452c6ccf
出典データセット
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04018824

反応ノート

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