Butanal → 2-Propyl-1,3-dioxane
反応式
[CH:1](=[O:5])[CH2:2][CH2:3][CH3:4].[CH2:6](O)[CH2:7][CH2:8][OH:9].P(=O)(O)(O)O.C(=O)CCC.O>O>[CH2:2]([CH:1]1[O:9][CH2:8][CH2:7][CH2:6][O:5]1)[CH2:3][CH3:4]参加物
6
実験手順
Examples 5-7 were carried out using the apparatus described above. Prior to each example, the column was heated to 100° C. with boiling water as described above. Butyraldehyde was fed through the bottom feed plate and a mixture of 1,3-propanediol and 500 ppmw phosphoric acid was fed through the upper feed plate at rates described in Table II. A butyraldehyde/water azeotrope was condensed overhead at 73° C. The basepot reached a maximum temperature of 165° C. Material was removed from the basepot throughout the run. The material separated into two phases, each of which was analyzed by gas chromatography. The results are listed in Table II.
後処理
- customcondensed overhead at 73° C
- customa maximum temperature of 165° C
- customMaterial was removed from the basepot throughout the run
- customThe material separated into two phases
出典と根拠
- ORDレコード
- ord-e0b7be06a4da4f9fa669657fd48f9c2f
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09315485B2
反応ノート
読み込み中…