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Potassium Hydroxide → 3-ethoxy-5-phenylthiophene-2-carboxylic acid

HRID 621794
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반응식

HRID 621794 반응식
[CH2:1]([O:3][C:4]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[S:6][C:5]=1[C:15]([O:17]C)=[O:16])[CH3:2].[OH-].[K+]>O1CCCC1.O>[CH2:1]([O:3][C:4]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[S:6][C:5]=1[C:15]([OH:17])=[O:16])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 14154187HCID 14154187, 화합물

생성물 1

HCID 141541963-ethoxy-5-phenylthiophene-2-carboxylic acid수율 92.8%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of methyl 3-ethoxy-5-phenyl-2-thiophenecarboxylate (12.0 g, 46 mmoles) in tetrahydrofuran (150 mL) is added to a solution of potassium hydroxide (14.6 g, 229 mmoles) in water (150 mL). The mixture is stirred and heated under reflux for 24 hours, then the tetrahydrofuran is removed using a rotary evaporator. The aqueous suspension is cooled in an ice bath and acidified with concentrated HCl. The precipitate is collected by filtration, rinsed well with water and dried to afford the pure product (10.6 g); mp 174°-175° C.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 24 hours
  3. customthe tetrahydrofuran is removed
  4. customa rotary evaporator
  5. temperatureThe aqueous suspension is cooled in an ice bath
  6. filtrationThe precipitate is collected by filtration
  7. washrinsed well with water
  8. customdried

출처 및 근거

ORD 기록
ord-92f96a21e97c471db183d0e02d89d7c9
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824958

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