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Sodium Hydroxide → 3-(4-Phenylthiophen-2-yl)-2-thioxopropanoic acid

HRID 1397214
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HRID 1397214 반응식
[C:1]1([C:7]2[CH:8]=[C:9]([CH:12]=[C:13]3[S:17]C(=S)N[C:14]3=[O:19])[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-:20].[Na+]>O>[C:1]1([C:7]2[CH:8]=[C:9]([CH2:12][C:13](=[S:17])[C:14]([OH:19])=[O:20])[S:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 472983595-((4-Phenylthiophen-2-yl)methylene)-2-thioxothiazolidin-4-one

생성물 1

HCID 866775883-(4-Phenylthiophen-2-yl)-2-thioxopropanoic acid수율 74%

시약·촉매·용매 1

HCID 962Water용매

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온도
95 °C

실험 절차

A suspension of product 5-((4-phenylthiophen-2-yl)methylene)-2-thioxothiazolidin-4-one (1.4 g, 4.6 mmol) in 12 mL of 10% aqueous NaOH was heated to 95° C. for 1 h. The solution was cooled to room temperature and diluted with water. The aqueous phase was washed with EtOAc, and acidified with 10% HCl. The precipitate that was formed was filtered, washed with water and dried under reduced pressure to get the product 3-(4-phenylthiophen-2-yl)-2-thioxopropanoic acid (0.9 g, yield 74%). MS (ESI) m/z: Calculated for C13H10O2S2: 262.01. found: 261.0 (M−H)−. The crude product was carried through without further purification

후처리

  1. temperatureThe solution was cooled to room temperature
  2. washThe aqueous phase was washed with EtOAc
  3. customThe precipitate that was formed
  4. filtrationwas filtered
  5. washwashed with water
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-eb4daf333b924b258f8aa2a2a6fee004
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901156B2

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