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Dibenzyl-trans-hex-3-ene-1,6-dioate → trans-beta-Hydromuconic acid

HRID 128489
ノート
印刷プレビュー

反応式

HRID 128489 の反応式
C([O:8][C:9](=[O:24])[CH2:10]/[CH:11]=[CH:12]/[CH2:13][C:14]([O:16]CC1C=CC=CC=1)=[O:15])C1C=CC=CC=1>[OH-].[Na+]>[C:14]([OH:16])(=[O:15])[CH2:13]/[CH:12]=[CH:11]/[CH2:10][C:9]([OH:24])=[O:8]
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 1

HCID 11438713Dibenzyl-trans-hex-3-ene-1,6-dioate

生成物 1

HCID 5351896trans-beta-Hydromuconic acid収率 34.7%

試薬・触媒・溶媒 1

HCID 14798Sodium Hydroxide溶媒

実験手順

A suspension of 1.62 grams (5.00 mmoles) of dibenzyl-trans-hex-3-ene-1,6-dioate in 25 ml of 10% sodium hydroxide solution is heated to reflux for 12 hours. At the end of this time the reaction mixture is cooled and extracted twice, each with 15 ml of chloroform. The aqueous phase is acidified with dilute hydrochloric acid and extracted three times with 50 ml portions of ether. The ether extracts are combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Recrystallization of the yellowish residual oil from aqueous methanol yields 0.25 gram of trans-hex-3-ene-1,6-dioic acid, m.p.=197°-198° C. (Lit. m.p.=199°). The melting point of a mixture of the reaction product and an authentic sample obtained from Aldrich Chemical Co. remains unchanged.

後処理

  1. temperatureis heated
  2. temperatureto reflux for 12 hours
  3. temperatureAt the end of this time the reaction mixture is cooled
  4. extractionextracted twice
  5. extractionextracted three times with 50 ml portions of ether
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customRecrystallization of the yellowish residual oil from aqueous methanol

出典と根拠

ORDレコード
ord-ce2fb69e97cc43d6aad68baba94e9879
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04259519

反応ノート

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