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Diethyl Ether → HCID 178467026, 화합물

HRID 2419798
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HRID 2419798 반응식
I.[NH2:2][NH:3][C:4]([NH:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[NH:5].C(OCC)C.[OH-].[Na+].[CH2:21]([O:23][C:24]1[CH:31]=[C:30]([O:32][CH2:33][CH3:34])[CH:29]=[C:28]([O:35][CH2:36][CH3:37])[C:25]=1[CH:26]=O)[CH3:22]>C(Cl)Cl.CCCCCC>[CH2:7]([NH:6][C:4]([NH:3][N:2]=[CH:26][C:25]1[C:24]([O:23][CH2:21][CH3:22])=[CH:31][C:30]([O:32][CH2:33][CH3:34])=[CH:29][C:28]=1[O:35][CH2:36][CH3:37])=[NH:5])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 2897412,4,6-TriethoxybenzaldehydeHCID 178506603HCID 178506603, 화합물

생성물 1

HCID 178467026HCID 178467026, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 8058
Hexane
용매

실험 절차

A mixture of 10.0 g. of 1-amino-3-benzylguanidine hydroiodide and 100 ml. each of diethyl ether, n-hexane and methylene chloride is shaken with 10 ml. of 5N NaOH. To this is added 8.15 g. of 2,4,6-triethoxybenzaldehyde and the mixture is shaken for 15 minutes. The organic layer is washed with saturated aqueous sodium chloride, passed through hydrous sodium magnesium silicate and concentrated to dryness under reduced pressure. The residue is crystallized from aqueous ethanol, giving the desired product as nearly colorless crystals, m.p. 140°-141° C.

후처리

  1. additionA mixture of 10.0 g
  2. additionTo this is added 8.15 g
  3. washThe organic layer is washed with saturated aqueous sodium chloride
  4. concentrationconcentrated to dryness under reduced pressure
  5. customThe residue is crystallized from aqueous ethanol

출처 및 근거

ORD 기록
ord-0bccac6b643f4a81b1df27788c0938aa
출처 데이터셋
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04107326

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