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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 57435847, 화합물

HRID 33389
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반응식

HRID 33389 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[C:3]=1[NH:10][C:11](=[O:15])[O:12][CH2:13][CH3:14].C(N(CC)CC)C.Cl[C:24]([O:27]C(Cl)=O)(Cl)Cl>ClCCl>[CH3:9][O:8][C:4]1[C:3]2[N:10]([C:11]([O:12][CH2:13][CH3:14])=[O:15])[C:24](=[O:27])[NH:1][C:2]=2[CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10426DiphosgeneHCID 86603973Ethyl (2-amino-6-methoxy-phenyl)-carbamate

생성물 1

HCID 57435847HCID 57435847, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

13.0 g (0.062 mol) ethyl (2-amino-6-methoxy-phenyl)-carbamate and 10.3 mL (0.074 mol) triethylamine in 100 mL dichloromethane are added to a solution of 8.20 mL (0.068 mol) trichloromethylchloroformate in 50 mL dichloromethane while cooling with ice. After 4 hours stirring at ambient temperature the reaction mixture is poured onto ice and extracted with dichloromethane. The combined organic phases are washed with water, dried and freed from the solvent. The residue is stirred in diethyl ether.

후처리

  1. temperaturewhile cooling with ice
  2. additionis poured onto ice
  3. extractionextracted with dichloromethane
  4. washThe combined organic phases are washed with water
  5. customdried
  6. stirringThe residue is stirred in diethyl ether

출처 및 근거

ORD 기록
ord-eaa408e68e90459c97843c8f9c84f0bf
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429583B2

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