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

HRID 1397214
ノート
印刷プレビュー

反応式

HRID 1397214 の反応式
[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
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

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
95 °C

実験手順

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

後処理

  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

出典と根拠

ORDレコード
ord-eb4daf333b924b258f8aa2a2a6fee004
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901156B2

反応ノート

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