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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl Isocyanate → N-Methyl 3-phenoxy-1-azetidinecarboxamide

HRID 903129
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HRID 903129 반응식
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]
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참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-2ea87a6f475d4ea68b6f25720e31af84
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04226861

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