Phosphorus oxide (P4O10) → 4H,5H,6H-cyclopenta(b)thiophen-6-one

HRID 2091572

反応式

HRID 2091572 の反応式
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[S:15]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][C:22]([OH:24])=O)=[CH:16]1>CS(O)(=O)=O>[S:15]1[CH:19]=[CH:18][C:17]2[CH2:20][CH2:21][C:22](=[O:24])[C:16]1=2

参加物

4

反応物 2

HCID 14812Phosphorus oxide (P4O10)HCID 2689183-(Thiophen-3-yl)propanoic acid

生成物 1

HCID 3156144H,5H,6H-cyclopenta(b)thiophen-6-one収率 30.3%

試薬・触媒・溶媒 1

HCID 6395Methanesulfonic Acid溶媒

実験手順

To a suspension of P2O5 (25.4 g, 179.0 mmol) in methanesulfonic acid (100 mL) was added 3-(thiophen-3-yl)propanoic acid (5.0 g, 32.0 mmol) and the reaction was stirred at room temperature for 1 h. At completion, the reaction was concentrated and the residue was purified by flash chromatography (20-30% EtOAc/hexane eluent) to give 4H-cyclopenta[b]thiophen-6(5H)-one (1.34 g, 30% yield) as a brown solid. 1H NMR (300 MHz, MeOH) δ ppm 8.14 (d, J=4.8 Hz, 1H), 7.17 (d, J=4.8 Hz, 1H), 2.94-3.15 (m, 4H); MS (EI) m/z=139.2 [M+1]+.

後処理

  1. concentrationAt completion, the reaction was concentrated
  2. customthe residue was purified by flash chromatography (20-30% EtOAc/hexane eluent)

出典と根拠

ORDレコード
ord-0c365191e08a423e92d919537cddc9e9
出典データセット
uspto-grants-2013_05
特許番号
US08440652B2

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