Methyl 4,4,4-trifluoro-2-hydroxybutanoate → 4,4,4-Trifluoro-2-hydroxybutanamide
反応式
[F:1][C:2]([F:11])([F:10])[CH2:3][CH:4]([OH:9])[C:5](OC)=[O:6].[NH3:12].CO>>[F:1][C:2]([F:11])([F:10])[CH2:3][CH:4]([OH:9])[C:5]([NH2:12])=[O:6]参加物
3
実験手順
A solution of 12-3 (200 mg, 1.16 mmol) in 7N NH3/MeOH (10 mL) was heated at 70° C. overnight. The reaction mixture was filtered, and the filtrate was concentrated to dryness. The residue was dissolved in 1,2-dimethoxyethane (10 mL) and filtered to remove insolubles. The filtrate was concentrated to dryness to afford Intermediate 12. 1H NMR (500 MHz, DMSO-d6) δ 7.40 (br s, 1H), 7.34 (br s, 1H), 5.93 (m, 1H), 4.10 (m, 1H), 2.64-2.65 (m, 1H), 2.40-2.41 (m, 1H).
後処理
- filtrationThe reaction mixture was filtered
- concentrationthe filtrate was concentrated to dryness
- dissolutionThe residue was dissolved in 1,2-dimethoxyethane (10 mL)
- filtrationfiltered
- customto remove insolubles
- concentrationThe filtrate was concentrated to dryness
出典と根拠
- ORDレコード
- ord-20dbfbff0a8c4a75b6880e7ff4c3a084
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09428492B2
反応ノート
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