Ammonium Chloride → Cyclohexyl(6-fluoro-3-methyl-1-benzofuran-2-yl)methanol

HRID 2091145ノート

反応式

HRID 2091145 の反応式
[F:1][C:2]1[CH:13]=[CH:12][C:5]2[C:6]([CH3:11])=[C:7]([CH:9]=[O:10])[O:8][C:4]=2[CH:3]=1.[CH:14]1([Mg]Br)[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1.[Cl-].[NH4+]>O1CCCC1>[CH:14]1([CH:9]([C:7]2[O:8][C:4]3[CH:3]=[C:2]([F:1])[CH:13]=[CH:12][C:5]=3[C:6]=2[CH3:11])[OH:10])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 823743336-Fluoro-3-methyl-1-benzofuran-2-carbaldehydeHCID 178419651HCID 178419651、化合物

生成物 1

HCID 66778852Cyclohexyl(6-fluoro-3-methyl-1-benzofuran-2-yl)methanol収率 67%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution (20 mL) of 6-fluoro-3-methyl-1-benzofuran-2-carbaldehyde (940 mg) synthesized above in tetrahydrofuran was added a 1.0M solution (7.92 mL) of cyclohexylmagnesium bromide in tetrahydrofuran at 0° C., and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, tetrahydrofuran was evaporated in an evaporator, and the residue was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (15% ethyl acetate/hexane) to give the title object compound (931 mg, 67%) as a pale-yellow oil.

後処理

  1. customto quench
  2. customthe reaction, tetrahydrofuran
  3. customwas evaporated in an evaporator
  4. extractionthe residue was extracted with ethyl acetate
  5. washThe extract was washed with saturated brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by silica gel column chromatography (15% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-7c15a985818a4855bbbc36f722a39a1d
出典データセット
uspto-grants-2013_05
特許番号
US08436043B2

反応ノート

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