Methyl Isocyanate → 1-[1-(4-Bromo-phenyl)ethyl]-3-methyl-urea

HRID 858577

반응식

HRID 858577 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH2:10])[CH3:9])=[CH:4][CH:3]=1.[CH3:11][N:12]=[C:13]=[O:14]>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH:10][C:13]([NH:12][CH3:11])=[O:14])[CH3:9])=[CH:4][CH:3]=1

참가 물질

4

반응물 2

HCID 12228Methyl IsocyanateHCID 853000(R)-4-bromo-alpha-methylbenzylamine

생성물 1

HCID 471273271-[1-(4-Bromo-phenyl)ethyl]-3-methyl-urea수율 94%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
25 °C

실험 절차

To a stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.5 g, 2.49 mmol) in anhydrous CH2Cl2 was added methyl isocyanate (0.15 mL, 2.49 mmol). The resulting solution was stirred at 25° C. overnight. CH2Cl2 was evaporate and residue partitioned between EtOAC and 1 N HCl. The organic layer was washed with H2O, brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (80% EtOAc in hexanes) to provide the desired product (0.60 g, 94%) as a white solid.

후처리

  1. customCH2Cl2 was evaporate
  2. customresidue partitioned between EtOAC and 1 N HCl
  3. washThe organic layer was washed with H2O, brine
  4. dry with materialdried over Na2SO4
  5. customThe solvent was removed in vacuo
  6. customthe residue was purified by flash column chromatography (80% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-2ab5911dda914485bf2df388fee5d0f1
출처 데이터셋
uspto-grants-2006_12
특허 번호
US07148226B2

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