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(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triol → Rosin erucic acid

HRID 32783
ノート
印刷プレビュー

反応式

HRID 32783 の反応式
[CH:1]1[CH:6]=[CH:5][C:4](/[CH:7]=[CH:8]/[CH2:9][O:10][C@@H:11]2[O:16][C@H:15]([CH2:17][OH:18])[C@@H:14]([OH:19])[C@H:13]([OH:20])[C@H:12]2[OH:21])=[CH:3][CH:2]=1.[C:22]([OH:45])(=[O:44])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]/[CH:34]=[CH:35]\[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]>>[CH:1]1[CH:2]=[CH:3][C:4](/[CH:7]=[CH:8]/[CH2:9][O:10][C@@H:11]2[O:16][C@H:15]([CH2:17][OH:18])[C@@H:14]([OH:19])[C@H:13]([OH:20])[C@H:12]2[OH:21])=[CH:5][CH:6]=1.[C:22]([OH:45])(=[O:44])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]/[CH:34]=[CH:35]\[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 5280656(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triolHCID 5281116Erucic Acid

生成物 1

HCID 131727065Rosin erucic acid収率 253.1%

実験手順

Into a 1000 mL reaction vessel equipped with a stirrer, a thermometer and a gas-introducing tube were charged 47 g (0.14 mol) of hydrogenated rosin (KP-610, manufactured by Arakawa Chemical Industries, Ltd.), 48 g (0.14 mol) of erucic acid, 160 g (0.28 mol) of dimerdiol (PESPOL HP-1000, manufactured by TOAGOSEI Co. Ltd.). After inner air was replaced with nitrogen, a dehydration was conducted at 240° C. for 15 hours under a nitrogen flow. After cooling, unreacted acids were removed with an aqueous sodium hydroxide solution. The resulting mixture was washed with water, and heptane, the solvent in the mixture, was distilled off to obtain 225 g of aimed hydrogenated rosin/erucic acid dimerdiol ester. The obtained hydrogenated rosin/erucic acid dimerdiol ester is in a liquid state at a normal temperature, and its acid value and hydroxyl value were 0.1 and 7.6, respectively.

後処理

  1. customInto a 1000 mL reaction vessel
  2. customequipped with a stirrer
  3. temperatureAfter cooling
  4. customunreacted acids were removed with an aqueous sodium hydroxide solution
  5. washThe resulting mixture was washed with water, and heptane
  6. distillationthe solvent in the mixture, was distilled off

出典と根拠

ORDレコード
ord-91fcc78562d849bba7a0b9f3945ab662
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07427640B1

反応ノート

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