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Methyl 1-(5-bromopyridin-3-yl)cyclopropanecarboxylate → HCID 66788306, 화합물

HRID 2407438
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HRID 2407438 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8]2([C:11]([O:13]C)=[O:12])[CH2:10][CH2:9]2)[CH:5]=[N:6][CH:7]=1.O([Si](C)(C)C)[K:16]>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([C:8]2([C:11]([O-:13])=[O:12])[CH2:9][CH2:10]2)[CH:5]=[N:6][CH:7]=1.[K+:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 59578399Methyl 1-(5-bromopyridin-3-yl)cyclopropanecarboxylateHCID 178504318HCID 178504318, 화합물

생성물 1

HCID 66788306HCID 66788306, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of methyl 1-(5-bromopyridin-3-yl)cyclopropanecarboxylate (1 g, 3.9 mmol) in THF (40 mL) was added 90% KOTMS (0.557 g, 3.9 mmol), and the mixture was stirred at room temperature overnight. The mixture was filtered and washed with THF to give potassium 1-(5-bromopyridin-3-yl)cyclopropanecarboxylate. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.63-0.69 (m, 2H), 1.09-1.15 (m, 2H), 7.79-7.80 (m, 1H), 8.34-8.37 (m, 2H).

후처리

  1. filtrationThe mixture was filtered
  2. washwashed with THF

출처 및 근거

ORD 기록
ord-d53acf07f0f24ca69bbe048d2ad1c7d4
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08809545B2

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