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Phosphorus sulfide (P2S5) → 8-Fluoro-2,2-dimethyl-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-thione

HRID 633354
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HRID 633354 반응식
[F:1][C:2]1[C:7]2[O:8][C:9]([CH3:14])([CH3:13])[C:10](=O)[NH:11][C:6]=2[CH:5]=[C:4]([N+:15]([O-:17])=[O:16])[CH:3]=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:19]>C1COCC1>[F:1][C:2]1[C:7]2[O:8][C:9]([CH3:14])([CH3:13])[C:10](=[S:19])[NH:11][C:6]=2[CH:5]=[C:4]([N+:15]([O-:17])=[O:16])[CH:3]=1
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참가 물질

4

반응물 2

HCID 14817Phosphorus sulfide (P2S5)HCID 898638688-Fluoro-2,2-dimethyl-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-one

생성물 1

HCID 898638698-Fluoro-2,2-dimethyl-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-thione수율 69%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 8-Fluoro-2,2-dimethyl-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-one (0.75 g, 3.1 mmol) in 25 ml anhydrous THF, P2S5 (2.8 g, 6.25 mmol) was added and the reaction mixture was heated to reflux for 12 hours. Analysis of LC-MS indicated the completion of the reaction. Volatiles were removed in vacuo and the crude reaction mixture was partitioned in EtOAc (100 ml) and saturated aqueous NH4Cl (100 ml). Layers were separated and the organic layer was washed (×2) with saturated aqueous NH4Cl (50 ml). EtOAc layer was dried over Na2SO4 and concentrated to give the product in 69% yield (0.55 g). LCMS (m/z) 257 (MH+).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 12 hours
  3. customthe completion of the reaction
  4. customVolatiles were removed in vacuo
  5. customthe crude reaction mixture
  6. customwas partitioned in EtOAc (100 ml)
  7. customLayers were separated
  8. washthe organic layer was washed (×2) with saturated aqueous NH4Cl (50 ml)
  9. dry with materialEtOAc layer was dried over Na2SO4
  10. concentrationconcentrated
  11. customto give the product in 69% yield (0.55 g)

출처 및 근거

ORD 기록
ord-7a49b07a8168480ca06d05e84451caef
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09321763B2

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