Chlorosuccinimide → HCID 20351119, 화합물

HRID 2052571노트

반응식

HRID 2052571 반응식
[CH3:1][S:2][CH:3]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[NH:5][C:4]1=[O:15].[Cl:16]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[Cl:16][C:3]1([S:2][CH3:1])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[NH:5][C:4]1=[O:15]

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 3266503-Methylthio-5-nitrooxindole

생성물 1

HCID 20351119HCID 20351119, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of 3-methylthio-5-nitrooxindole (900 mg, 4 mmol) and N-chlorosuccinimide (600 mg, 4.5 mmol) in 50 ml of chloroform was stirred at room temperature for 1 hour and then evaporated to dryness in vacuo, yielding 3-chloro-3-methylthio-5-nitrooxindole. The residue was dissolved in 15 ml of tetrahydrofuran and added to a vigorously stirred slurry of red mercuric oxide powder (900 mg, 4.3 mmol) and boron trifluoride etherate (600 mg, 4.3 mmol) in 100 ml of 20 percent aqueous tetrahydrofuran. After stirring at room temperature for two hours, the reaction mixture was extracted with three 100-ml portions of chloroform. The chloroform layer was dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was recrystallized from 95 percent ethanol to give 5-nitroisatin (600 mg, 78%), mp 252°-254°

후처리

  1. customevaporated to dryness in vacuo

출처 및 근거

ORD 기록
ord-a6c32b1252c6452695737de16ebcfd2b
출처 데이터셋
uspto-grants-1980_01
특허 번호
US04186132

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