反応式
[CH2:1]([C:3]1[O:4][CH2:5][CH2:6][N:7]=1)[CH3:2].[CH2:8]=[O:9]>O>[OH:9][CH2:8][CH:1]([C:3]1[O:4][CH2:5][CH2:6][N:7]=1)[CH3:2]参加物
実験手順
As an example, step A was conducted by reacting 2-ethyl-2-oxazoline (4 moles) having less than 1,000 ppm of water with paraformaldehyde (1 mole) at a reaction temperature of 100° C. for approximately 5.5 hours. The excess oxazoline reactant was removed along with water as "overheads" by fractional distillation of the reaction product, leaving the 2-(α-hydroxymethylethyl)-2-oxazoline in approximately 96 percent yield. Step C was then conducted by continuously adding the 2-(α-hydroxymethylethyl)-2-oxazoline to a stirred solution of sodium hydroxide in the mono-methyl ether of triethylene glycol at a temperature of from 100°-105° C. Under these conditions, the 2-isopropenyl-2-oxazoline and water were volatilized and recovered from the overheads. The product yield was approximately 98 percent of theory.
後処理
- customat a reaction temperature of 100° C.
- customfor approximately 5.5 hours
- customThe excess oxazoline reactant was removed along with water as "overheads" by fractional distillation of the reaction product
出典と根拠
- ORDレコード
- ord-cc80b9ad742a44a68b171e00a1d87ef7
- 出典データセット
- uspto-grants-1983_03
- 特許番号
- US04376861
関連ノート
読み込み中…