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Potassium ethylxanthate → HCID 20736364, 화합물

HRID 1072696
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HRID 1072696 반응식
Br[CH:2]([C:4]1[O:5][C:6](=[O:11])[C:7]([CH3:10])([CH3:9])[N:8]=1)[CH3:3].[K+].[CH2:13]([O:15][C:16]([S-:18])=[S:17])[CH3:14]>C(#N)C>[CH2:13]([O:15][C:16](=[S:17])[S:18][CH:2]([C:4]1[O:5][C:6](=[O:11])[C:7]([CH3:10])([CH3:9])[N:8]=1)[CH3:3])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2735045Potassium ethylxanthateHCID 22253674HCID 22253674, 화합물

생성물 1

HCID 20736364HCID 20736364, 화합물수율 81.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 2-(1-bromo-ethyl)-4,4-dimethyl-4H-oxazol-5-one (3.00 g; 13.6 mmol) and 50 mL acetonitrile was added O-ethyl xanthic acid potassium salt (2.18 g; 13.6 mmol). The mixture was stirred under a nitrogen atmosphere at room temperature for 5 hours. The reaction mixture was filtered and the solid was washed with 10 mL acetontrile 10 mL. The combined filtrate was concentrated under reduced pressure to afford 2.89 g (81%) of dithiocarbonic acid S-[1-(4,4-dimethyl-5-oxo-4,5-dihydro-oxazol-2-yl)-ethyl]ester O-ethyl ester as a yellow oil.

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후처리

  1. filtrationThe reaction mixture was filtered
  2. washthe solid was washed with 10 mL acetontrile 10 mL
  3. concentrationThe combined filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-015db7d52cfb4890adb709e4d86444aa
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06911510B2

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