Toluene → 1,2-Hexadecanediol Oleyl Alcohol

HRID 1719658

反応式

HRID 1719658 の反応式
[CH2:1]([OH:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[CH2:20]([OH:37])[CH:21]([OH:36])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35].C1(C)C=CC=CC=1.B(O)(O)O>O>[CH2:20]([OH:37])[CH:21]([OH:36])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35].[CH2:1]([OH:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

参加物

6

反応条件

温度
65 °C

実験手順

Approximately 54 g of oleyl alcohol, 51 g of 1,2-hexadecanediol and 100 g of toluene were reacted in a 1 liter reaction equipped as described in Example 1. The contents were heated to about 65° C. and 13 g of boric acid were added. The mixture was further heated up to 155° C. over a period of 4 hours until water evolution stopped. Approximately 11 ml. of water were collected by azeotropic distillation. The solvent was removed by vacuum distillation at 155° C. and the product was filtered at 90°-100° C. through diatomaceous earth.

後処理

  1. customequipped
  2. distillationof water were collected by azeotropic distillation
  3. customThe solvent was removed by vacuum distillation at 155° C.
  4. filtrationthe product was filtered at 90°-100° C. through diatomaceous earth

出典と根拠

ORDレコード
ord-41215c991e4f41bf9a161a9fc1497b32
出典データセット
uspto-grants-1985_09
特許番号
US04541941

関連ノート

読み込み中…