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Methylamine → HCID 19836622, 화합물

HRID 476846
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HRID 476846 반응식
[CH3:1][C:2]1([CH3:13])[CH2:4][N:3]1[P:5](Br)([N:7]1[CH2:9][C:8]1([CH3:11])[CH3:10])=[S:6].[CH3:14][NH2:15]>C1COCC1>[CH3:1][C:2]1([CH3:13])[CH2:4][N:3]1[P:5]([N:7]1[CH2:9][C:8]1([CH3:11])[CH3:10])(=[S:6])[NH:15][CH3:14]
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참가 물질

4

반응물 2

HCID 6329MethylamineHCID 54098565HCID 54098565, 화합물

생성물 1

HCID 19836622HCID 19836622, 화합물수율 65%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In a similar manner 0.025 moles of P,P-bis(2,2-dimethyl-1-aziridinyl)thiophosphinic bromide in about 170 milliliters of THF, prepared in accordance with Example 1, is saturated with an excess of gaseous methylamine, kept overnight at 4° C., filtered, concentrated on a rotary evaporator at room temperature, and vacuum distilled to provide about 65% yield of P,P-bis(2,2-dimethyl-1-aziridinyl)-N methylthiophosphinic amide.

후처리

  1. filtrationfiltered
  2. concentrationconcentrated on a rotary evaporator at room temperature
  3. distillationvacuum distilled

출처 및 근거

ORD 기록
ord-213cc3ff20f0414b9f45dcbb8e927f15
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04886790

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