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4-Nitrobenzenesulfonyl chloride → Aziridine, 1-((4-nitrophenyl)sulfonyl)-

HRID 598862
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HRID 598862 반응식
[NH:1]1[CH2:3][CH2:2]1.C(=O)(O)[O-].[Na+].[N+:9]([C:12]1[CH:17]=[CH:16][C:15]([S:18](Cl)(=[O:20])=[O:19])=[CH:14][CH:13]=1)([O-:11])=[O:10]>C(Cl)(Cl)Cl>[N+:9]([C:12]1[CH:13]=[CH:14][C:15]([S:18]([N:1]2[CH2:3][CH2:2]2)(=[O:20])=[O:19])=[CH:16][CH:17]=1)([O-:11])=[O:10]
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참가 물질

5

반응물 3

HCID 74044-Nitrobenzenesulfonyl chlorideHCID 9033AziridineHCID 516892Sodium Bicarbonate

생성물 1

HCID 148462Aziridine, 1-((4-nitrophenyl)sulfonyl)-

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a 25 mL round-bottom flask was added aziridine (10 mg, 234 μmol), sodium bicarbonate (20 mg, 234 μmol), 4-nitrobenzene-1-sulfonyl chloride (45 mg, 234 μmol) and 2 mL chloroform. After 10 minutes, LC-MS showed the desired product was formed. The reaction mixture was concentrated under reduced pressure to give the crude product of the title compound, that was used directly for the next step. MS m/z: 229 (M+1).

출처 및 근거

ORD 기록
ord-c91c4c20f35947b1b765f07b60d00a92
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897619B2

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