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N-methylbenzohydrazide → N-methylbenzoselenohydrazide

HRID 420117
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HRID 420117 반응식
[CH3:1][N:2]([C:4](=O)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[NH2:3].C1C=CC(P2([Se]P(C3C=CC=CC=3)(=[Se])[Se]2)=[Se:19])=CC=1>C1(C)C=CC=CC=1>[CH3:1][N:2]([C:4](=[Se:19])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[NH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 242395N-methylbenzohydrazideHCID 50660752,4-Diphenyl-1,3,2,4-diselenadiphosphetane 2,4-diselenide

생성물 1

HCID 57551066N-methylbenzoselenohydrazide수율 194.7%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of N-methylbenzohydrazide (450 mg, 3.0 mmol) and the Woollins' Reagent (540 mg, 1 mmol) in anhydrous toluene (10 ml), was heated at 120° C. for Ih. The resulting orange solution was cooled to room temperature, the solvent was removed in vacuo and the selenoamide purified by column chromatography on silica gel (3:1 Hexane:EtOAc) and to give N-methylbenzoselenohydrazide (415 mg) in 65% yield.

후처리

  1. customthe solvent was removed in vacuo
  2. customthe selenoamide purified by column chromatography on silica gel (3:1 Hexane:EtOAc)

출처 및 근거

ORD 기록
ord-9dccb36e76e740d6baae2c152a49a0c9
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08093425B2

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