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

HRID 128489
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HRID 128489 반응식
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]
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참가 물질

3

반응물 1

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

생성물 1

HCID 5351896trans-beta-Hydromuconic acid수율 34.7%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-ce2fb69e97cc43d6aad68baba94e9879
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04259519

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