Thionyl Chloride → 2-Chloro-1,3-benzoxazol-6-OL

HRID 1635657ノート

反応式

HRID 1635657 の反応式
S[C:2]1[O:3][C:4]2[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:5]=2[N:6]=1.S(Cl)([Cl:14])=O>CN(C)C=O>[Cl:14][C:2]1[O:3][C:4]2[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:5]=2[N:6]=1

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 178515778HCID 178515778、化合物

生成物 1

HCID 234412462-Chloro-1,3-benzoxazol-6-OL

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2-Sulfanyl-1,3-benzoxazol-6-ol (2.08 g) [see Preparation 33] was added to thionyl chloride (12.3 ml), followed by dimethylformamide (0.93 ml). The reaction mixture was heated to reflux for 5 minutes, after which time the mixture was allowed to cool. The solvent was removed under reduced pressure, the residue azeotroped twice with xylene, and the residue then partitioned between diethyl ether and water. The organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 0:100, by volume, hexane:ethyl acetate in 50% increments to afford 2-chloro-1,3-benzoxazol-6-ol (1.715 g) as a white solid.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 5 minutes
  3. temperatureto cool
  4. customThe solvent was removed under reduced pressure
  5. customthe residue azeotroped twice with xylene
  6. customthe residue then partitioned between diethyl ether and water
  7. customThe organic layer was separated
  8. dry with materialdried over magnesium sulphate
  9. customthe solvent removed under reduced pressure
  10. customThe crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 0:100, by volume, hexane

出典と根拠

ORDレコード
ord-b2537be91fa04978b951a7c30d0b3961
出典データセット
uspto-grants-2003_01
特許番号
US06509464B1

反応ノート

読み込み中…