Water → {5-[4-(Trifluoromethyl)phenyl]isoxazol-3-yl}methan-1-ol

HRID 1827889ノート

反応式

HRID 1827889 の反応式
[F:1][C:2]([F:20])([F:19])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:13][N:12]=[C:11]([C:14](OCC)=[O:15])[CH:10]=2)=[CH:5][CH:4]=1.[BH4-].[Na+].O>C(O)C>[F:20][C:2]([F:1])([F:19])[C:3]1[CH:4]=[CH:5][C:6]([C:9]2[O:13][N:12]=[C:11]([CH2:14][OH:15])[CH:10]=2)=[CH:7][CH:8]=1

参加物

5

反応物 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 22064085Ethyl 5-(4-(trifluoromethyl)phenyl)isoxazole-3-carboxylate

生成物 1

HCID 22064161{5-[4-(Trifluoromethyl)phenyl]isoxazol-3-yl}methan-1-ol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
0 °C

実験手順

Ethyl 5-[4-(trifluoromethyl)phenyl]isoxazole-3-carboxylate (130 mg) was dissolved in ethanol (10 ml), cooled to 0° C., and sodium borohydride (26 mg) was added in portions to the stirred solution. The mixture was stirred at room temperature for 4 hours, then excess water added. Solvent was evaporated under reduced pressure, and the residue was purified by preparative thin layer chromatography, eluting with 5% methanol/ethyl acetate, to provide {5-[4-(trifluoromethyl)phenyl]isoxazol-3-yl}methan-1-ol, a compound of formula (24).

後処理

  1. customSolvent was evaporated under reduced pressure
  2. customthe residue was purified by preparative thin layer chromatography
  3. washeluting with 5% methanol/ethyl acetate

出典と根拠

ORDレコード
ord-6ed58539a59b4818a1b8e1cf869fa4f8
出典データセット
uspto-grants-2006_06
特許番号
US07056924B2

反応ノート

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