Methanol → HCID 20388954、化合物
反応式
[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])=[CH:5][N:6]=1.S(=O)(=O)(O)O.[CH3:17]O>>[CH3:1][C:2]1[S:3][C:4]([CH2:7][CH2:8][C:9]([O:11][CH3:17])=[O:10])=[CH:5][N:6]=1参加物
4
実験手順
A mixture of 31.7 g of the product of Step B, 3.2 ml of concentrated sulfuric acid and 300 ml of methanol was refluxed for 16 hours and was evaporated to dryness under reduced pressure. The residue was taken up in 100 ml of water and concentrated ammonium hydroxide was added thereto to adjust the pH to 12-13. The mixture was extracted with methylene chloride and the extracts were dried over magnesium sulfate and evaporated to dryness under reduced pressure to obtain 35 g of raw methyl 2-methyl-5-thiazole-propanoate. Reaction with hydrochloric acid resulted in the hydrochloride melting at 115° C.
後処理
- temperaturewas refluxed for 16 hours
- customwas evaporated to dryness under reduced pressure
- additionconcentrated ammonium hydroxide was added
- extractionThe mixture was extracted with methylene chloride
- dry with materialthe extracts were dried over magnesium sulfate
- customevaporated to dryness under reduced pressure
出典と根拠
- ORDレコード
- ord-24817f9474c342b28b22206343f173d9
- 出典データセット
- uspto-grants-1979_10
- 特許番号
- US04172137
反応ノート
読み込み中…