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Dichloromethane → HCID 19002930, 화합물

HRID 2259506
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인쇄 미리보기

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HRID 2259506 반응식
C[Si](C)(C)[C:3]1[O:11][C:10]2[C:5](=[N:6][C:7]([CH3:12])=[CH:8][CH:9]=2)C=1.[Cl:15]N1C(=O)N(Cl)C(=O)N(Cl)C1=O.CCOC(C)=O.[CH2:33]([Cl:35])Cl>CCCCCC>[Cl:15][C:3]1[O:11][C:10]2[C:5](=[N:6][C:7]([CH3:12])=[CH:8][CH:9]=2)[C:33]=1[Cl:35]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 6909Trichloroisocyanuric AcidHCID 8857Ethyl AcetateHCID 114356745-Methyl-2-trimethylsilanyl-furo[3,2-b]pyridine

생성물 1

HCID 19002930HCID 19002930, 화합물수율 96%

시약·촉매·용매 1

HCID 8058Hexane용매

반응 조건

온도
0 °C

실험 절차

To a solution of 2-trimethylsilyl-5-methylfurano[3,2-b]pyridine (1.05 g, 5.15 mmol) in CH2Cl2 (16 mL) at 0° C. was added trichloroisocyanuric acid (1.2 g, 5.15 mmol). The mixture was stirred at 0° C. for 30 rain and then at r.t. for 20 hr. A solution of 30% EtOAc in hexane was added. The resulting mixture was filtered through a short bed of silica gel and eluted with more 30% EtOAc in hexane. Evaporation of the filtrate gave 1.0 g (96%) of the title compound.

후처리

  1. filtrationThe resulting mixture was filtered through a short bed of silica gel
  2. washeluted with more 30% EtOAc in hexane
  3. customEvaporation of the filtrate

출처 및 근거

ORD 기록
ord-0b2b9cb5b35d403da2a02636feebfe8b
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05472964

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