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Methanol → HCID 59173400, 화합물

HRID 220095
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HRID 220095 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([CH:14]=C)[CH:13]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7].C[OH:19]>>[CH:14]([C:12]1[CH:11]=[C:5]([CH:4]=[C:3]([C:2]([F:17])([F:16])[F:1])[CH:13]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[O:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 887MethanolHCID 59173387Ethyl 3-trifluoromethyl-5-vinylbenzoate

생성물 1

HCID 59173400HCID 59173400, 화합물

반응 조건

온도
-78 °C

실험 절차

25.39 g (103.96 mmol) of ethyl 3-(trifluoromethyl)-5-vinylbenzoate 33 is dissolved in dry MeOH (200 mL) and reaction vessel Is cooled down to −78° C. Then O3 is bubbled through for 1.5 hours until the reaction mixture turned dark blue. Then ozone is turned off and nitrogen is bubbled through the reaction mixture to remove extra ozone from the solution. 9.6 g of dimethyl sufide (155.95 mmol, 1.5 eq) is added and the reaction mixture is stirred at −78° C. for 2 hours followed by at room temperature for another hour. All the solvents are removed and ethyl 3-formyl-5-(trifluoromethyl)benzoate 34 is isolated via flash column chromatography (5-10% EtOAc/Hex). MS: m/z [M+H+]) 247.18, 1H NMR 10.16 (s, 1H), 8.73 (s, 1H), 8.56, (s, 1H), 8.35 (s, 1H), 4.46-4.51 (q, 2H, J=7.21 Hz), 1.45-1.49 (t, 3H, J=7.21 Hz).

후처리

  1. customreaction vessel
  2. customThen O3 is bubbled through for 1.5 hours until the reaction mixture
  3. customnitrogen is bubbled through the reaction mixture
  4. customto remove extra ozone from the solution
  5. addition9.6 g of dimethyl sufide (155.95 mmol, 1.5 eq) is added
  6. waitfollowed by at room temperature for another hour
  7. customAll the solvents are removed

출처 및 근거

ORD 기록
ord-709e1f68a4d047c18ed2d0876545f1db
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202876B2

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