Sodium Hydroxide → Phenyl(pyridazin-4-yl)methanone

HRID 339710

反応式

HRID 339710 の反応式
[CH2:1]([C:8]1[CH:13]=[CH:12][N:11]=[N:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-:14].[Na+]>C(O)(=O)C>[C:2]1([C:1]([C:8]2[CH:13]=[CH:12][N:11]=[N:10][CH:9]=2)=[O:14])[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 5984154-Benzylpyridazine

生成物 1

HCID 12486783Phenyl(pyridazin-4-yl)methanone

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

反応条件

温度
100 °C

実験手順

To a 100° C. suspension of SeO2 (4.75 g, 0.043 mole) in acetic acid (216 mL) was added dropwise to a solution of 4-benzylpyridazine (11; 7.6 g, 0.044.6 mole) in acetic acid (216 mL). The mixture was heated for 1 hour at 100° C. The reaction mixture was cooled to room temperature and was neutralized to a pH ˜6-7 with 50% NaOH. The neutralized mixture was extracted twice with CH2Cl2. The combined extracts were dried over MgSO4 and were evaporated to dryness. The crude product was purified by crystallization in refluxing isopropyl alcohol (10 vol). The yield of phenylpyridazin-4-yl-methanone (12) obtained was 5.8 g or 66%. MS (ESI+): [M+H]+=185.33; 1H NMR (300 MHz, CDCl3), δ ppm: 7.5-7.60 (m, 2H), 7.64-7.83 (m, 4H), 9.42-9.51 (m, 2H).

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionThe neutralized mixture was extracted twice with CH2Cl2
  3. dry with materialThe combined extracts were dried over MgSO4
  4. customwere evaporated to dryness
  5. customThe crude product was purified by crystallization
  6. temperaturein refluxing isopropyl alcohol (10 vol)

出典と根拠

ORDレコード
ord-7d2ea79406194ab58aad7f311b3f3114
出典データセット
uspto-grants-2014_11
特許番号
US08895556B2

関連ノート

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