Thionyl Chloride → HCID 178458779、化合物

HRID 2236538ノート

反応式

HRID 2236538 の反応式
O[CH2:2][C:3]1[CH:8]=[C:7]([OH:9])[C:6]([O:10][CH2:11][CH2:12][CH3:13])=[CH:5][N:4]=1.S(Cl)([Cl:16])=O>C(Cl)(Cl)Cl>[Cl:16][CH2:2][C:3]1[CH:8]=[C:7]([OH:9])[C:6]([O:10][CH2:11][CH2:12][CH3:13])=[CH:5][N:4]=1

参加物

4

実験手順

To a mixture of 2-hydroxymethyl-5-propoxy-pyridin-4-ol (5.56 g, 30.3 mmole) and 30 mL of chloroform stirred cooled with an ice bath is added 30 mL of thionyl chloride (x g, 0.x mole). This is stirred for 15 minutes at ice bath temperature and then refluxed for 1 hour. The reaction mixture is cooled, evaporated to dryness in vacuo and then treated with isopropanol. The solid is filtered, washed with fresh isopropanol, then ether and air dried to give an off-white solid, 3.4 g, (48%), m.p. 165-7° C.; MS (ES+): m/z 202.3 (M+H).

後処理

  1. temperaturecooled with an ice bath
  2. stirringThis is stirred for 15 minutes at ice bath temperature
  3. temperaturerefluxed for 1 hour
  4. temperatureThe reaction mixture is cooled
  5. customevaporated to dryness in vacuo
  6. additiontreated with isopropanol
  7. filtrationThe solid is filtered
  8. washwashed with fresh isopropanol
  9. dry with materialether and air dried
  10. customto give an off-white solid, 3.4 g, (48%), m.p. 165-7° C.

出典と根拠

ORDレコード
ord-66f1ec9bb0884da8a56ede6feae45b90
出典データセット
uspto-grants-2010_05
特許番号
US07713994B2

反応ノート

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