Phosphorus pentachloride → 2-Chloro-5-phenylbenzoxazole

HRID 1815755

反応式

HRID 1815755 の反応式
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13](=S)[NH:12][C:11]=3[CH:16]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:18]>P(Cl)(Cl)(Cl)=O>[Cl:18][C:13]1[O:14][C:10]2[CH:9]=[CH:8][C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[CH:16][C:11]=2[N:12]=1

参加物

4

反応物 2

HCID 24819Phosphorus pentachlorideHCID 30326635-Phenyl-2(3H)-benzoxazolethione

生成物 1

HCID 141698182-Chloro-5-phenylbenzoxazole収率 640.1%

試薬・触媒・溶媒 1

HCID 24813Phosphorus oxychloride溶媒

実験手順

5-Phenyl-3H-benzooxazole-2-thione (227 mg, 1.0 mmol) was dissolved in phosphorus oxychloride (1.6 mL). Phosphorus pentachloride (208 mg, 1.0 mmol) was added and the mixture was placed in an oil bath at 100° C. for 3 h. The mixture was allowed to cool to RT and concentrated. The crude residue was concentrated from CH2Cl2 (3×). The crude reaction product was triturated with hexanes (40 mL), and the resulting solids were collected by filtration. The solids were washed with hexanes (20 mL×3) and dried to afford 1.47 g (73%) of the title compound: 1H NMR (CDCl3, 400 MHz) δ 7.86 (d, 1H, J=1.3 Hz), 7.60-7.56 (m, 3H), 7.55-7.52 (m, 1H), 7.49-7.44 (m, 2H), 7.40-7.36 (m, 1H); 13C NMR (CDCl3, 100 MHz) δ 151.6, 151.4, 141.9, 140.7, 139.3, 129.2, 127.8, 127.7, 125.2, 118.4, 110.7; MS (Cl) m/z 230.1 (M+1); HPLC retention time=5.41 min.

後処理

  1. concentrationconcentrated
  2. concentrationThe crude residue was concentrated from CH2Cl2 (3×)
  3. customThe crude reaction product
  4. customwas triturated with hexanes (40 mL)
  5. filtrationthe resulting solids were collected by filtration
  6. washThe solids were washed with hexanes (20 mL×3)
  7. customdried

出典と根拠

ORDレコード
ord-8bc6c6de71bc402f866dccdc05727d65
出典データセット
uspto-grants-2005_04
特許番号
US06881734B2

関連ノート

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