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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 5372577, 화합물 → HCID 12840254, 화합물

HRID 2190086
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HRID 2190086 반응식
[CH:1]([Mg]Br)([CH3:3])[CH3:2].[C:6]([O:16][CH3:17])(=[O:15])/[CH:7]=[CH:8]/[CH2:9][CH2:10][C:11]([O:13]C)=O>C1COCC1>[CH:1]([CH:8]1[CH2:9][CH2:10][C:11](=[O:13])[CH:7]1[C:6]([O:16][CH3:17])=[O:15])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 5372577HCID 5372577, 화합물HCID 178418365HCID 178418365, 화합물

생성물 1

HCID 12840254HCID 12840254, 화합물수율 101.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

An isopropylmagnesium bromide (58 mL, 58 mmol) solution (15% in THF, ˜1 M) was treated with Cu(I)I (0.28 g, 1.5 mmol) and cooled to 0° C. A solution of (E)-dimethyl hex-2-enedioate (5.0 g, 29 mmol; See Example 80, Step 1) was added dropwise, and the solution was stirred at 0° C. for an additional 30 minutes and then at room temperature. The product was poured into saturated NHCl4 (250 mL) with rapid stirring. The mixture was extracted into DCM. The combined organics were back extracted with H2O, and dried with MgSO4, filtered, and concentrated under reduced pressure to yield methyl 2-isopropyl-5-oxocyclopentanecarboxylate (5.4 g, 100%), which was used without further purification. 1H NMR (CDCl3, 400 MHz) δ 3.76-3.73 (m, 3H), 2.94-2.91 (m, 1H), 2.48-2.16 (m, 2H), 1.87-1.84 (m, 2H), 1.68-1.43 (m, 2H), 0.97-0.84 (m, 6H).

후처리

  1. customat room temperature
  2. extractionThe mixture was extracted into DCM
  3. extractionThe combined organics were back extracted with H2O
  4. dry with materialdried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e5a3c5a08445476fb92f9afa7b4fab72
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324221B2

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