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Sodium Carbonate → 5-(4-Fluoro-phenyl)-thiomorpholine-3-thione

HRID 539622
ノート
印刷プレビュー

反応式

HRID 539622 の反応式
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:2].C(=O)([O-])[O-].[Na+].[Na+].[F:21][C:22]1[CH:27]=[CH:26][C:25]([CH:28]2[NH:33][C:32](=O)[CH2:31][S:30][CH2:29]2)=[CH:24][CH:23]=1>C1COCC1>[F:21][C:22]1[CH:27]=[CH:26][C:25]([CH:28]2[NH:33][C:32](=[S:2])[CH2:31][S:30][CH2:29]2)=[CH:24][CH:23]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10340Sodium CarbonateHCID 14817Phosphorus sulfide (P2S5)HCID 582002835-(4-Fluoro-phenyl)-thiomorpholin-3-one

生成物 1

HCID 582003125-(4-Fluoro-phenyl)-thiomorpholine-3-thione収率 63%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A mixture of phosphorus pentasulfide (5.12 g, 11.5 mmol) and sodium carbonate (1.22 g, 11.5 mmol) in THF (30 mL) was stirred at room temperature. A solution of 5-(4-fluoro-phenyl)-thiomorpholin-3-one (2.0 g, 9.5 mmol) in THF (25 mL) was slowly added, and the mixture was stirred at room temperature for 90 minutes. The mixture was diluted with 10% aqueous Na3PO4 solution (40 mL), and stirred at room temperature for five minutes. The mixture was extracted with a 1:4 mixture of ethyl acetate and diethyl ether, and the organic phase was separated, dried over MgSO4, filtered and concentrated under reduced pressure. Elution of the residue through silica (15-20% ethyl acetate/hexanes) gave 1.36 g of 5-(4-fluoro-phenyl)-thiomorpholine-3-thione, MP=107-108° C.

後処理

  1. stirringthe mixture was stirred at room temperature for 90 minutes
  2. stirringstirred at room temperature for five minutes
  3. extractionThe mixture was extracted with a 1:4 mixture of ethyl acetate and diethyl ether
  4. customthe organic phase was separated
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. washElution of the residue through silica (15-20% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-16ce7495b3464151b09de987fcc0ca7e
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871760B2

反応ノート

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