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Ethylene Glycol → HCID 90004235, 화합물

HRID 587861
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HRID 587861 반응식
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][C@@H:4]([C:12]([O:14][CH3:15])=[O:13])[CH2:3]1.[CH2:16](O)[CH2:17][OH:18].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1C=CC=CC=1>[C:2]12([O:18][CH2:17][CH2:16][O:1]1)[C:11]1[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=1)[CH2:5][C@@H:4]([C:12]([O:14][CH3:15])=[O:13])[CH2:3]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 90004151HCID 90004151, 화합물

생성물 1

HCID 90004235HCID 90004235, 화합물수율 85.9%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To the stirred solution of (R)-methyl 4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate (4.5 g, 22.03 mmol) in benzene (40 mL), ethane-1,2-diol (3.69 mL, 66.1 mmol) and a catalytic amount of p-toluenesulfonic acid was added. The reaction mixture was heated to reflux temperature and further maintained for 20 hours. After 20 hours, the reaction mixture was allowed to RT, concentrated under vacuum to yield 12 g of crude compound. Crude material was purified by flash chromatography (Biotage) using 7% ethyl acetate:hexane get title compound (4.7 g) m/z 248.6.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux temperature
  3. temperaturefurther maintained for 20 hours
  4. customwas allowed to RT
  5. concentrationconcentrated under vacuum
  6. customto yield 12 g of crude compound
  7. customCrude material was purified by flash chromatography (Biotage)

출처 및 근거

ORD 기록
ord-a5a7373482e14d21a31c0dc2f62d4cd1
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227919B2

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