Hydrochloric Acid → 2-(Carboxymethoxy)thioxanthone

HRID 899421

反応式

HRID 899421 の反応式
[OH-].[Na+].[OH:3][C:4]1[CH:17]=[CH:16][C:15]2[S:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:18])[C:6]=2[CH:5]=1.[Na].Br[CH2:21][C:22]([O:24]CC)=[O:23].Cl>O1CCCC1.O>[C:22]([CH2:21][O:3][C:4]1[CH:17]=[CH:16][C:15]2[S:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:18])[C:6]=2[CH:5]=1)([OH:24])=[O:23]

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 7748Ethyl bromoacetateHCID 14798Sodium HydroxideHCID 5360545SodiumHCID 97945682-Hydroxy-9H-thioxanthen-9-one2 回

生成物 1

HCID 30198532-(Carboxymethoxy)thioxanthone

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

24 g sodium hydroxide was refluxed in 400 ml tetrahydrofuran for five minutes. 22.8 g (0.1 mols) 2-hydroxythioxanthone was added and reflux was continued for 1 hour, during which time the colour changed to bright red, indicating the formation of the sodium salt of 2-hydroxythioxanthone. 35.1 g (0.21 mols) of ethyl bromoacetate was added and reflux was continued for three hours. After cooling to room temperature, 400 ml of deionised water was added, with stirring, and the tetrahydrofuran was distilled out to yield a clear red solution. Reflux was continued for a further 2 hours in order to hydrolyse all the ester intermediate. The solution was then cooled to 50° C., and 400 ml 1.0 M hydrochloric acid was added, with stirring, causing the solid product to precipitate out. After refluxing for a further five minutes to be sure that all the sodium salt was converted to free acid, the solution was cooled to room temperature and stirred for two hours before filtering off the solid, washing with 400 ml deionised water and drying in a vacuum oven at 80° C.

後処理

  1. temperaturereflux
  2. temperaturereflux
  3. waitwas continued for three hours
  4. distillationthe tetrahydrofuran was distilled out
  5. customto yield a clear red solution
  6. temperatureReflux
  7. waitwas continued for a further 2 hours in order
  8. temperatureThe solution was then cooled to 50° C.
  9. stirringwith stirring
  10. customto precipitate out
  11. temperatureAfter refluxing for a further five minutes
  12. temperaturethe solution was cooled to room temperature
  13. stirringstirred for two hours
  14. filtrationbefore filtering off the solid
  15. washwashing with 400 ml
  16. customdrying in a vacuum oven at 80° C.

出典と根拠

ORDレコード
ord-98502927409346a2b432102c6d631c00
出典データセット
uspto-grants-2008_04
特許番号
US07354957B2

関連ノート

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