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Allyl bromide → N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea

HRID 1111021
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HRID 1111021 반응식
[OH:1][N:2]=[C:3]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]([NH:14][CH2:15][C:16]([O:18][CH:19]([CH3:21])[CH3:20])=[O:17])=[O:13])=[CH:7][CH:6]=1)[CH3:4].C[O-].[Na+].[CH2:25](Br)[CH:26]=[CH2:27]>O>[CH2:27]([O:1][N:2]=[C:3]([C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12]([NH:14][CH2:15][C:16]([O:18][CH:19]([CH3:21])[CH3:20])=[O:17])=[O:13])=[CH:9][CH:10]=1)[CH3:4])[CH:26]=[CH2:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 10942334Sodium MethoxideHCID 72742602N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea

생성물 1

HCID 54128761N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of the N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea in 25% methanolic sodium methoxide (1.0 equivalent) is treated at room temperature with 1.1 equivalent of allyl bromide. The reaction mixture is stirred until the temperature falls to about 20° C. The reaction mixture is then poured into cold water and extracted with diethyl ether. The ether solution is dried over MgSO4 and filtered, and the solvent is removed by rotary evaporator to yield the product N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea.

후처리

  1. customfalls to about 20° C
  2. extractionextracted with diethyl ether
  3. dry with materialThe ether solution is dried over MgSO4
  4. filtrationfiltered
  5. customthe solvent is removed by rotary evaporator

출처 및 근거

ORD 기록
ord-ca254232c13e4cf6a5976595cec640d0
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04977272

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