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

HRID 1739452
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반응식

HRID 1739452 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 1133Thioglycolic AcidHCID 1376632,5-Difluorobenzaldehyde

생성물 1

HCID 9014395-Fluoro-1-benzothiophene-2-carboxylic acid수율 80.1%

시약·촉매·용매 2

HCID 962Water용매2회HCID 14797Potassium Hydroxide용매

반응 조건

온도
125 °C

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-8597088b936b4e00b8463565dad44c73
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05965749

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