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Ethylene Glycol → 1-(1,3-Dioxolane-2-yl)-3,3,3-trifluoropropane-2-one

HRID 869111
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HRID 869111 반응식
[CH2:1]([O:3][CH:4]=[CH:5][C:6](=[O:11])[C:7]([F:10])([F:9])[F:8])[CH3:2].C(O)C[OH:14]>C1(C)C=CC=CC=1.O.CC1C=CC(S(O)(=O)=O)=CC=1>[O:3]1[CH2:1][CH2:2][O:14][CH:4]1[CH2:5][C:6](=[O:11])[C:7]([F:9])([F:10])[F:8]
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참가 물질

5

반응물 2

HCID 174Ethylene GlycolHCID 27803954-Ethoxy-1,1,1-trifluoro-3-buten-2-one

생성물 1

HCID 552960491-(1,3-Dioxolane-2-yl)-3,3,3-trifluoropropane-2-one수율 67.3%

시약·촉매·용매 2

HCID 521998p-Toluenesulfonic acid monohydrate촉매HCID 1140Toluene용매

실험 절차

4-Methylbenzenesulfonic acid monohydrate (500.1 mg, 467.4 μL, 2.629 mmol) was added to a solution of 4-ethoxy-1,1,1-trifluoro-but-3-en-2-one (200.97 g, 1.195 mol) and ethylene glycol (77.27 g, 69.42 mL, 1.245 mol) in toluene (502.5 mL). The reaction mixture was heated to reflux for 90 min (oil bath). Then, the reflux was continued with simultaneous distillation of ethanol/toluene. The Dean-Stark was removed and the flask was connected to a distillation apparatus. 3-(1,3-Dioxolan-2-yl)-1,1,1-trifluoro-propan-2-one was distilled using a KNF pump (Bp 81° C.) as a light yellow oil (148 g, 67% yield). 1H NMR (500 MHz, CDCl3) δ 5.38-5.40 (t, 1H), 4.02-4.05 (m, 2H), 3.93-3.95 (m, 2H), 3.10 (d, 2H).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 90 min (oil bath)
  3. distillationThen, the reflux was continued with simultaneous distillation of ethanol/toluene
  4. customThe Dean-Stark was removed
  5. distillation3-(1,3-Dioxolan-2-yl)-1,1,1-trifluoro-propan-2-one was distilled

출처 및 근거

ORD 기록
ord-443b33f208db4f75bbb860460b077ca0
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969360B2

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