反応式
OO.[CH3:3][S:4][CH2:5][C:6]1[N:11]=[C:10]([OH:12])[C:9]([CH3:13])=[C:8]([CH3:14])[N:7]=1.CC[O:17]CC>C(O)(=O)C>[CH3:3][S:4]([CH2:5][C:6]1[N:11]=[C:10]([OH:12])[C:9]([CH3:13])=[C:8]([CH3:14])[N:7]=1)=[O:17]参加物
5
実験手順
6.8 g (0.1 mol) of 50% strength hydrogen peroxide were added to a mixture of 18.4 g (0.1 mol) of 2-methylthiomethyl-4-hydroxy-5,6-dimethylpyrimidine in 100 ml of glacial acetic acid at 10° C. The mixture was subsequently stirred for 3 hours, without cooling, about 300 ml of ether were added and the product which had precipitated was filtered off. 17 g (85% of theory) of 2-methysulphinylmethyl-4-hydroxy-5,6-dimethylpyrimidine were thus obtained in the form of a grey powder with a melting point of 112° C. ##STR7##
後処理
- temperaturewithout cooling
- customthe product which had precipitated
- filtrationwas filtered off
出典と根拠
- ORDレコード
- ord-9e5355ceecc2404b9ab66c2cbd785817
- 出典データセット
- uspto-grants-1980_11
- 特許番号
- US04234587
関連ノート
読み込み中…