Potassium Carbonate → 2-Hydroxy-1,3-benzothiazole-6-carboxylic acid

HRID 1393684

反応式

HRID 1393684 の反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[SH:11].[C:12](=O)([O-])[O-:13].[K+].[K+].ClC(Cl)(OC(=O)OC(Cl)(Cl)Cl)Cl>O1CCCC1>[O:13]=[C:12]1[NH:1][C:2]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=2[S:11]1

参加物

5

実験手順

4-Amino-3-mercaptobenzoic acid (680 mg) was dissolved in tetrahydrofuran (20 ml), and potassium carbonate (550 mg) was added thereto and stirred for 30 minutes at room temperature. The mixture was cooled to −78° C., and triphosgene (400 mg) was added thereto and stirred for 1 hour. The mixture was warmed to room temperature and concentrated under reduced pressure until the volume of the solvent became ⅓. Water (20 ml) and formic acid were added to the concentrate until it became acidic, and precipitated crystals were collected by filtration and washed with water and n-hexane. The crystals were dried under reduced pressure to give the title compound (740 mg, Y.:95%) as white crystals.

後処理

  1. temperatureThe mixture was cooled to −78° C.
  2. stirringstirred for 1 hour
  3. temperatureThe mixture was warmed to room temperature
  4. concentrationconcentrated under reduced pressure until the volume of the solvent
  5. additionWater (20 ml) and formic acid were added to the
  6. concentrationconcentrate until it
  7. customprecipitated crystals
  8. filtrationwere collected by filtration
  9. washwashed with water and n-hexane
  10. customThe crystals were dried under reduced pressure

出典と根拠

ORDレコード
ord-94ef4221512d495fbec3be3264be954f
出典データセット
uspto-grants-2008_03
特許番号
US07345180B2

関連ノート

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