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Methyl Isocyanate → N-Methyl 3-phenoxy-1-azetidinecarboxamide

HRID 903129
ノート
印刷プレビュー

反応式

HRID 903129 の反応式
CS([O-])(=O)=O.[O:6]([CH:13]1[CH2:16][NH:15][CH2:14]1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[OH-].[Na+].[CH3:19][N:20]=[C:21]=[O:22]>C1C=CC=CC=1>[CH3:19][NH:20][C:21]([N:15]1[CH2:16][CH:13]([O:6][C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:14]1)=[O:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 12228Methyl IsocyanateHCID 14798Sodium HydroxideHCID 85257MethanesulfonateHCID 128125013-Phenoxyazetidine

生成物 1

HCID 13420164N-Methyl 3-phenoxy-1-azetidinecarboxamide

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

The methanesulfonate of 3-phenoxyazetidine (10.5 g., 0.043 mole) was partitioned between 50 ml of benzene and 25 ml. of dilute sodium hydroxide. The benzene layer was dried over calcium sulfate and filtered. The filtrate was treated with 2.6 g. (0.043 mole) of methylisocyanate and the solution was stirred at room temperature for 18 hours. The resulting mixture was concentrated at reduced pressure and the residue was crystallized from a mixture of ethyl acetate-isopropyl ether to give 1.2 g. (14%) of product (m.p. 139°-141° C.).

後処理

  1. dry with materialThe benzene layer was dried over calcium sulfate
  2. filtrationfiltered
  3. additionThe filtrate was treated with 2.6 g
  4. concentrationThe resulting mixture was concentrated at reduced pressure
  5. customthe residue was crystallized from a mixture of ethyl acetate-isopropyl ether
  6. customto give 1.2 g

出典と根拠

ORDレコード
ord-2ea87a6f475d4ea68b6f25720e31af84
出典データセット
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04226861

反応ノート

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