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

HRID 2230016ノート

反応式

HRID 2230016 の反応式
[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]

参加物

6

反応条件

温度
70 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-4271d863b26b402c9facb1a2b299c343
出典データセット
uspto-grants-2002_07
特許番号
US06423690B1

反応ノート

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