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Diethylphosphite → 1-Carbomethoxymethyl-2-Diethoxyphosphoryl Hydrazine

HRID 1395395
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HRID 1395395 반응식
[C:1]([N:4](C)[NH:5][P:6]([O:11][CH2:12][CH3:13])([O:8][CH2:9][CH3:10])=[O:7])(=O)[CH3:2].Cl.CNNC[C:20](O)=[O:21].C([O:25]P([O-])OCC)C>>[C:2]([CH2:1][NH:4][NH:5][P:6]([O:11][CH2:12][CH3:13])([O:8][CH2:9][CH3:10])=[O:7])([O:21][CH3:20])=[O:25]
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참가 물질

4

반응물 3

HCID 3780918DiethylphosphiteHCID 203392921-Acetyl-1-Methyl-2-Diethoxyphosphoryl HydrazineHCID 714375282-(2-Methylhydrazinyl)acetic acid;hydrochloride

생성물 1

HCID 203392931-Carbomethoxymethyl-2-Diethoxyphosphoryl Hydrazine

실험 절차

This compound was synthesized in a similar manner to the compound of Example 5, except that methylhydrazinoacetate hydrochloride was used in place of 1-acetyl-1-methyl hydrazine and diethylphosphite was used in place of dimethylphosphite. A colorless oil was obtained which was subsequently distilled at 115° C./0.05 mm. to yield the desired product, nD27 =1.4342.

후처리

  1. customA colorless oil was obtained which
  2. distillationwas subsequently distilled at 115° C./0.05 mm

출처 및 근거

ORD 기록
ord-ce30004598534f7686ed1267d82c77a3
출처 데이터셋
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04203932

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