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2-Naphthylamine → 2-Naphthylurethane

HRID 1729319
노트
인쇄 미리보기

반응식

HRID 1729319 반응식
[CH2:1]([O:3][C:4](Cl)=[O:5])[CH3:2].[CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1[NH2:17].C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl.C(Cl)Cl.O>[CH2:1]([O:3][C:4]([NH:17][C:8]1[CH:9]=[CH:10][C:11]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=1)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 70572-NaphthylamineHCID 10928Ethyl chloroformateHCID 516892Sodium Bicarbonate

생성물 1

HCID 6119952-Naphthylurethane수율 84%

시약·촉매·용매 3

HCID 962Water용매HCID 6212Chloroform용매
HCID 6344
Dichloromethane
용매
2회

실험 절차

A mixture of 16.7 g of ethoxycarbonyl chloride and 20 ml of methylene chloride is added dropwise to a mixture of 20.0 g of 2-naphthylamine, 17.6 g of sodium bicarbonate, 100 ml of water and 200 ml of methylene chloride under ice-cooling and stirring. The mixture is stirred overnight at room temperature. Chloroform is added to the mixture and the organic layer is separated, dried and treated with charcol. The residue is recrystallized from ethyl acetate-hexane to give 25.26 g of N-ethoxycarbonyl-2-naphthylamine.

후처리

  1. temperaturecooling
  2. stirringThe mixture is stirred overnight at room temperature
  3. customthe organic layer is separated
  4. customdried
  5. additiontreated with charcol
  6. customThe residue is recrystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-95b3a56ca5cf4691b932be2e8b04a40d
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05332754

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