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

HRID 869111
ノート
印刷プレビュー

反応式

HRID 869111 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 521998p-Toluenesulfonic acid monohydrate触媒HCID 1140Toluene溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-443b33f208db4f75bbb860460b077ca0
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969360B2

反応ノート

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