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Ethyl diazoacetate → HCID 86732070, 화합물

HRID 1498809
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HRID 1498809 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([CH:8]=[CH2:9])[N:5]=[C:4]([CH3:10])[N:3]=1.[N+](=[CH:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])=[N-]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[N:3]=[C:4]([CH3:10])[N:5]=[C:6]([CH:8]2[CH2:9][CH:13]2[C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12192Ethyl diazoacetateHCID 86732069HCID 86732069, 화합물

생성물 1

HCID 86732070HCID 86732070, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A solution of 4-chloro-2-methyl-6-vinylpyrimidine (4-1, 15.0 g, 97 mmol 1.0 eq) in Toluene (300 mL) was heated to 100° C. under a nitrogen atmosphere. A solution of ethyl diazoacetate (30.2 mL, 291 mmol, 3.0 eq) was added as a solution in toluene (100 mL) over 1.5 hours. Heating was continued for 2 hours. The reaction mixture was allowed to cool to room temperature and concentrated to dryness. The residue was partitioned between saturated sodium bicarbonate solution (1 L) and ethyl acetate (1 L). The organic layer was separated, dried over sodium sulfate, filtered and concentrated to dryness. The resulting residue was purified by silica gel column chromatography (0-100% ethyl acetate in hexanes) to give ethyl 2-(6-chloro-2-methylpyrimidin-4-yl)cyclopropanecarboxylate (4-2) as a colorless oil.

후처리

  1. temperatureHeating
  2. concentrationconcentrated to dryness
  3. customThe residue was partitioned between saturated sodium bicarbonate solution (1 L) and ethyl acetate (1 L)
  4. customThe organic layer was separated
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness
  8. customThe resulting residue was purified by silica gel column chromatography (0-100% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-6fa7c06accc340b19a979dd3cee8283b
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09200001B2

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