Sodium Hydroxide → 5-Hydroxy-3-phenyl-5-(trifluoromethyl)-4,5-dihydroisoxazole

HRID 2262525

反応式

HRID 2262525 の反応式
[C:1]([CH2:9][C:10]([C:12]([F:15])([F:14])[F:13])=O)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:17][OH:18].[OH-:19].[Na+]>>[C:2]1([C:1]2[CH2:9][C:10]([OH:19])([C:12]([F:13])([F:14])[F:15])[O:18][N:17]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

4

反応物 3

HCID 14798Sodium HydroxideHCID 675894,4,4-Trifluoro-1-phenyl-1,3-butanedioneHCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 28809765-Hydroxy-3-phenyl-5-(trifluoromethyl)-4,5-dihydroisoxazole収率 91.5%

実験手順

Prepared according to J. Org. Chem., 1995, 60, 3907. A solution of benzoyltrifluoroacetone (21 g, 97 mmol) was added dropwise over 1 h, at 20-30° C., to a solution of hydroxylamine HCl (6.82 g, 98 mmol) containing sodium hydroxide (2 N, 51 mL, 102 mmol) and the resulting mixture heated under reflux for 45 min. After cooling to room temperature, the mixture was poured into ice-water (500 mL), the precipitate was filtered off, washed with water and dried under vacuum to afford the title compound (20.51 g, 91%) which was obtained as a white solid. MS: m/e=230.2 [M−H]−.

後処理

  1. customPrepared
  2. temperaturethe resulting mixture heated
  3. temperatureunder reflux for 45 min
  4. filtrationthe precipitate was filtered off
  5. washwashed with water
  6. customdried under vacuum

出典と根拠

ORDレコード
ord-5d15e887717e41d781e50743dbbb8b2b
出典データセット
uspto-grants-2010_12
特許番号
US07851469B2

関連ノート

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