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Thioglycolic Acid → 5-Fluoro-1-benzothiophene-2-carboxylic acid

HRID 1739452
ノート
印刷プレビュー

反応式

HRID 1739452 の反応式
F[C:2]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[CH:4]=O.[SH:11][CH2:12][C:13]([OH:15])=[O:14]>[OH-].[K+].O>[F:10][C:7]1[CH:8]=[CH:9][C:2]2[S:11][C:12]([C:13]([OH:15])=[O:14])=[CH:4][C:3]=2[CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 1133Thioglycolic AcidHCID 1376632,5-Difluorobenzaldehyde

生成物 1

HCID 9014395-Fluoro-1-benzothiophene-2-carboxylic acid収率 80.1%

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 14797Potassium Hydroxide溶媒

反応条件

温度
125 °C

実験手順

In a glass pressure bottle, 2,5-difluorobenzaldehyde (11 ml, 0.1 mol) was added to a solution of 2-mercaptoacetic acid (9 ml) in potassium hydroxide (16.5 g) and water (155 ml). The bottle was then sealed and heated in a hot oil bath to 125±5° C. for 1.25 hours. The bottle was then removed from the hot oil bath and cooled. A pale yellow precipitate was obtained in the bottle. At ambient temperature, the bottle was opened and sufficient water was added to dissolve the precipitate. The resultant aqueous material was washed with ether and then acidified with hydrochloric acid to produce a pale yellow solid. The pale yellow solid was collected on a filter, washed with water and dried, to produce 15.5 g of 5-fluoro-2-benzo-[b]thiophenecarboxylic acid (80.1% yield, mp>300° C.).

後処理

  1. customThe bottle was then sealed
  2. customThe bottle was then removed from the hot oil bath
  3. temperaturecooled
  4. customA pale yellow precipitate was obtained in the bottle
  5. customAt ambient temperature
  6. dissolutionto dissolve the precipitate
  7. washThe resultant aqueous material was washed with ether
  8. customto produce a pale yellow solid
  9. customThe pale yellow solid was collected on a filter
  10. washwashed with water
  11. customdried

出典と根拠

ORDレコード
ord-8597088b936b4e00b8463565dad44c73
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05965749

反応ノート

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