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Ethylene Glycol → HCID 19434044, 화합물

HRID 1736037
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HRID 1736037 반응식
[Br:1][C:2]1[CH:6]=[C:5]([Br:7])[S:4][C:3]=1[CH:8]=[O:9].[CH2:10](O)[CH2:11][OH:12]>C1(C)C=CC=CC=1.CC1C=CC(S(O)(=O)=O)=CC=1>[Br:1][C:2]1[CH:6]=[C:5]([Br:7])[S:4][C:3]=1[CH:8]1[O:12][CH2:11][CH2:10][O:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 174Ethylene GlycolHCID 8190403,5-Dibromothiophene-2-carbaldehyde

생성물 1

HCID 19434044HCID 19434044, 화합물수율 81%

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 1140Toluene용매

실험 절차

A mixture consisting of the product from Step A (11.0 g, 40.7 mmol), TsOH (0.25 g) and ethylene glycol (5.06 g, 81.5 mmol) in toluene (150 mL) was heated at reflux temperature for 1.5 h, water was removed by a Dean-Stark trap. The reaction mixture was cooled and poured into a saturared aqueous solution of sodium bicarbonate (100 mL). The organic layer was separated, dried (MgSO4), and evaporated to dryness. Purification of this crude material by column chromatography (silica, 6% ethyl acetate/hexane) gave 10.33 g of an oil (81%).

후처리

  1. temperaturewas heated
  2. temperatureat reflux temperature for 1.5 h
  3. customwater was removed by a Dean-Stark trap
  4. temperatureThe reaction mixture was cooled
  5. additionpoured into a saturared aqueous solution of sodium bicarbonate (100 mL)
  6. customThe organic layer was separated
  7. dry with materialdried (MgSO4)
  8. customevaporated to dryness
  9. customPurification of this crude material by column chromatography (silica, 6% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-8d264e1dad26489098f8308b37e4c13c
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05538966

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