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Succinic Acid → Succinic acid, di(2-octyl) ester

HRID 64504
ノート
印刷プレビュー

反応式

HRID 64504 の反応式
[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5].[CH3:9][CH:10](O)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].CS(O)(=O)=O>C1(C)C=CC=CC=1>[CH3:9][CH:10]([O:5][C:4](=[O:6])[CH2:3][CH2:2][C:1]([O:8][CH:10]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH3:9])=[O:7])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1110Succinic AcidHCID 6395Methanesulfonic AcidHCID 200832-Octanol

生成物 1

HCID 85861366Succinic acid, di(2-octyl) ester

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of succinic acid (Alfa-Aesar, 149.00 g, 1.26 mol), 2-octanol (Alfa-Aesar, 350.00 g, 2.69 mol), toluene (625 mL), and methanesulfonic acid (Alfa-Aesar, 2.00 g, 21 mmol) was heated to reflux for 6 hours. The water liberated was collected in a Dean Stark trap. The mixture was cooled, washed with saturated sodium bicarbonate (300 mL) and brine (100 mL), and dried over magnesium sulfate. The solvent was removed under vacuum to give a yellow oil that was used without further purification (426.39 g).

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 6 hours
  3. customThe water liberated was collected in a Dean Stark trap
  4. temperatureThe mixture was cooled
  5. washwashed with saturated sodium bicarbonate (300 mL) and brine (100 mL)
  6. dry with materialdried over magnesium sulfate
  7. customThe solvent was removed under vacuum
  8. customto give a yellow oil that
  9. customwas used without further purification (426.39 g)

出典と根拠

ORDレコード
ord-d9a54e4d69f34c5d96fd25a0d6324924
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447309B2

反応ノート

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