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Sodium Hydroxide → Stillingic acid

HRID 1385815
ノート
印刷プレビュー

反応式

HRID 1385815 の反応式
[OH-].[Na+].[C:3]([O:14]CC)(=[O:13])/[CH:4]=[CH:5]/[CH:6]=[CH:7]\[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>O1CCCC1>[C:3]([OH:14])(=[O:13])/[CH:4]=[CH:5]/[CH:6]=[CH:7]\[CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 5281162Ethyl 2,4-decadienoate, (2E,4Z)-

生成物 1

HCID 5282781Stillingic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

An aqueous solution of sodium hydroxide (10%, 22 ml) was added to a solution of technical grade ethyl (2E,4Z)-2,4-decadienoate (10 g) in tetrahydrofuran (100 ml). The mixture was heated under reflux for 5 hours with rapid stirring in a nitrogen atmosphere. After allowing to cool to room temperature, tetrahydrofuran was removed on a rotary evaporator, the residue was diluted with water (100 ml), and acidified to pH2 with 6N HCl. The acid was extracted with ether (3×100 ml) and the combined extracts were washed with water (2×50 ml) and brine (50 ml) and dried using anhydrous magnesium sulfate. Removal of ether under reduced pressure gave (2E,4Z)-2,4-decadienoic acid. This product was used in the next step without further purification.

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 5 hours
  3. customtetrahydrofuran was removed on a rotary evaporator
  4. additionthe residue was diluted with water (100 ml)
  5. extractionThe acid was extracted with ether (3×100 ml)
  6. washthe combined extracts were washed with water (2×50 ml) and brine (50 ml)
  7. customdried
  8. customRemoval of ether under reduced pressure

出典と根拠

ORDレコード
ord-750f1060a374474988c40a15d24f2db8
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06264939B1

反応ノート

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