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Water → 3-(2-Chloropyrimidin-4-yl)-6-methoxy-2-methylbenzaldehyde

HRID 873545
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HRID 873545 반응식
C(=O)([O-])[O-].[Na+].[Na+].[CH3:7][O:8][C:9]1[C:14]([CH:15]=[O:16])=[C:13]([CH3:17])[C:12](B2OC(C)(C)C(C)(C)O2)=[CH:11][CH:10]=1.[Cl:27][C:28]1[N:33]=[C:32](Cl)[CH:31]=[CH:30][N:29]=1.O>C(COC)OC>[Cl:27][C:28]1[N:33]=[C:32]([C:12]2[C:13]([CH3:17])=[C:14]([C:9]([O:8][CH3:7])=[CH:10][CH:11]=2)[CH:15]=[O:16])[CH:31]=[CH:30][N:29]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 775312,4-DichloropyrimidineHCID 130141572HCID 130141572, 화합물

생성물 1

HCID 1177007533-(2-Chloropyrimidin-4-yl)-6-methoxy-2-methylbenzaldehyde수율 88%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane
용매

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온도
80 °C

실험 절차

A 2 M aqueous solution of sodium carbonate (2.72 mL, 5.43 mol) and tetrakistriphenylphosphine palladium(0) (209 mg, 0.181 mmol) were added to a suspension of the 6-methoxy-2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde obtained in Example 4-1 (500 mg, 1.81 mmol) and 2,4-dichloropyrimidine (405 mg, 2.72 mmol) in dimethoxyethane (5.4 mL) at room temperature. The mixture thus obtained was stirred at 80° C. for 10 hours. Thereafter, the resulting solution was cooled to room temperature. Water was added to the reaction solution, and the precipitated crude product was collected by filtration and was then washed with water and diisopropyl ether to obtain the title compound (418 mg, yield: 88%).

후처리

  1. customThe mixture thus obtained
  2. temperatureThereafter, the resulting solution was cooled to room temperature
  3. customthe precipitated crude product
  4. filtrationwas collected by filtration
  5. washwas then washed with water and diisopropyl ether

출처 및 근거

ORD 기록
ord-10d6b4bbc5034e4f8f60272012c2420a
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08975263B2

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