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Methanol → Methyl 3-phenylmethylthiopyridine-4-carboxylate

HRID 1200013
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HRID 1200013 반응식
[C:1]1([CH2:7][C:8]2[CH:9]=[N:10][CH:11]=[CH:12][C:13]=2[C:14]([OH:16])=[S:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[CH3:22]O>COC(OC)(C)C>[C:1]1([CH2:7][C:8]2[CH:9]=[N:10][CH:11]=[CH:12][C:13]=2[C:14]([O:16][CH3:22])=[S:15])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 178526144HCID 178526144, 화합물

생성물 1

HCID 86742398Methyl 3-phenylmethylthiopyridine-4-carboxylate수율 96%

시약·촉매·용매 1

HCID 64952,2-Dimethoxypropane용매

실험 절차

A solution of 5.1 g (20 mmol) of 3-phenylmethylthiopyridine-4-carboxylic acid in 150 mL of methanol, 1.6 mL of 2,2-dimethoxypropane, and 5 mL of sulfuric acid was heated at reflux for 18 hours. The solution was cooled, concentrated to 25 mL, then partitioned between ether and sodium bicarbonate solution. The ether layer was washed with sodium bicarbonate solution, then brine, then dried and concentrated to afford 5.0 g (96%) of white crystals, m.p. 79°-80° C.

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후처리

  1. temperatureat reflux for 18 hours
  2. temperatureThe solution was cooled
  3. concentrationconcentrated to 25 mL
  4. custompartitioned between ether and sodium bicarbonate solution
  5. washThe ether layer was washed with sodium bicarbonate solution
  6. dry with materialbrine, then dried
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b6365abb9f4c4cbf8d9cd619bd7ac296
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04904672

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