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Methanol → HCID 59173400、化合物

HRID 220095
ノート
印刷プレビュー

反応式

HRID 220095 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

HCID 59173400HCID 59173400、化合物

反応条件

温度
-78 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-709e1f68a4d047c18ed2d0876545f1db
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08202876B2

反応ノート

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