Formaldehyde → 2-[(Ethylsulfanyl)methyl]prop-2-enoic acid

HRID 1005651노트

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HRID 1005651 반응식
[C:1](O)(=O)[CH2:2][C:3]([OH:5])=[O:4].C=O.C1(N[CH:17]2[CH2:22]CCCC2)CCCCC1.[CH2:23]([SH:25])C>O1CCOCC1>[CH2:22]([S:25][CH2:23][C:2](=[CH2:1])[C:3]([OH:5])=[O:4])[CH3:17]

참가 물질

6

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온도
70 °C

실험 절차

A mixture of malonic acid (5.2 g, 50 mmol), paraformaldehyde (3.3 g, 110 mmol), dicyclohexylamine, 9.95 ml, 50 mmol) and ethanethiol 4.06 ml, 55 mmol) in dioxane (120 ml) was heated at 70° C. for 2 hours. The solvents were removed under reduced pressure, the residue was redissolved in ethyl acetate and the solution was extracted with saturated aqueous sodium hydrogen carbonate (4×20 ml). The combined aqueous layers were washed with ethyl acetate (20 ml) then acidified with 1 M hydrochloric acid. The resulting suspension was extracted into dichloromethane and the solution was dried over anhydrous magnesium sulfate, filtered and evaporated to provide the title compound as a white solid (3.76 g, 52%). 1H-NMR; δ (CDCl3), 9.89 (1H, br s), 6.35 (1H, s), 5.77 (1H, s), 3.39 (2H, s), 2.49 (2H, dd, J=7.4, 14.5 Hz) and 1.25 (3H, t, J=5.2 Hz).

후처리

  1. customThe solvents were removed under reduced pressure
  2. dissolutionthe residue was redissolved in ethyl acetate
  3. extractionthe solution was extracted with saturated aqueous sodium hydrogen carbonate (4×20 ml)
  4. washThe combined aqueous layers were washed with ethyl acetate (20 ml)
  5. extractionThe resulting suspension was extracted into dichloromethane
  6. dry with materialthe solution was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-a052516570f5477581c67750fe57eb54
출처 데이터셋
uspto-grants-2004_09
특허 번호
US06787522B2

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