Triethylamine → 4-Cyano-2-methoxyphenyl trifluoromethanesulfonate

HRID 1038482ノート

反応式

HRID 1038482 の反応式
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([OH:11])=[C:7]([O:9][CH3:10])[CH:8]=1)#[N:2].C(N(CC)CC)C.[F:19][C:20]([F:26])([F:25])[S:21](Cl)(=[O:23])=[O:22].C(OCC)(=O)C>O1CCCC1.O>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([O:11][S:21]([C:20]([F:26])([F:25])[F:19])(=[O:23])=[O:22])=[C:7]([O:9][CH3:10])[CH:8]=1)#[N:2]

参加物

7

反応物 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 781354-Hydroxy-3-methoxybenzonitrileHCID 79000Trifluoromethanesulfonyl chloride

生成物 1

HCID 166592584-Cyano-2-methoxyphenyl trifluoromethanesulfonate収率 87%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-10 °C

実験手順

A mixture of 5-cyano-2-hydroxyanisole (600 mg, mmol) and triethylamine (1.40 mL, 10.0 mmol) was dissolved in anhydrous tetrahydrofuran (20 mL) under argon atomosphere. Trifluoromethanesulfonyl chloride (642 μL, 6.03 mmol) were added thereto at −10° C., and stirred at the same temperature for 1 hour. Ethyl acetate (100 mL) and water (100 mL) were added to the reaction mixture and partitioned. The organic layer was washed with saturated brine (50 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (979 mg) as a colorless solid. (Yield 87%)

後処理

  1. custompartitioned
  2. washThe organic layer was washed with saturated brine (50 mL)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was removed under reduced pressure
  5. customThe obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate)

出典と根拠

ORDレコード
ord-f2fd0ec01fe946ecabb23c6786ab8b63
出典データセット
uspto-grants-2013_10
特許番号
US08551991B2

反応ノート

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