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Ethylene Glycol → HCID 13137234, 화합물

HRID 1073699
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HRID 1073699 반응식
[CH3:1][C:2]1[O:13][C:5]([CH:6](O)[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[CH:4][CH:3]=1.C(O)C[OH:16].O.C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH2:7]([CH:6]1[C:2]([OH:13])([CH3:1])[CH:3]=[CH:4][C:5]1=[O:16])[CH2:8][CH2:9][CH2:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 174Ethylene GlycolHCID 962WaterHCID 517045Sodium AcetateHCID 11105991HCID 11105991, 화합물

생성물 1

HCID 13137234HCID 13137234, 화합물수율 84%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

In the same apparatus as in Example 1 5-methyl-α-n-pentyl-furfuryl alcohol (40 parts), ethylene glycol (20 parts) and a buffer solution prepared from water (1200 parts) and sodium acetate (0.5 part) and adjusted to pH 5.2 with acetic acid were charged, and the resultant mixture was stirred at 100° C. in a nitrogen stream for 20 hours. The reaction mixture was cooled and extracted with toluene. The extract was concentrated to give 2-n-pentyl-3-hydroxy-3-methyl-4-cyclopentenone in a yield of 84 %.

후처리

  1. additionwere charged
  2. temperatureThe reaction mixture was cooled
  3. extractionextracted with toluene
  4. concentrationThe extract was concentrated

출처 및 근거

ORD 기록
ord-cb5b018eb9824742bceda55fb5af5e7b
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04970345

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