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Ethyl xanthate → HCID 19876591, 화합물

HRID 1885977
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HRID 1885977 반응식
[CH2:1]([O:3][C:4]([SH:6])=[S:5])[CH3:2].[K].[C:8]([C:11]1[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=1[N+]#N)([OH:10])=[O:9].[B-](F)(F)(F)F>CC(C)=O>[Cl:17][C:16]1[C:11]([C:8]([OH:10])=[O:9])=[C:12]([S:5][C:4]([O:3][CH2:1][CH3:2])=[S:6])[CH:13]=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8823Ethyl xanthateHCID 26255TetrafluoroborateHCID 5462222PotassiumHCID 15059421HCID 15059421, 화합물

생성물 1

HCID 19876591HCID 19876591, 화합물

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

To a stirred suspension of 2.4 grams (0.014 mole) of ethylxanthic acid, potassium salt in 30 mL of acetone was added, by pipette, a stirred suspension of 2.0 grams (0.007 mole) of 2-carboxy-3-chlorobenzenediazonium tetrafluoborate in 50 mL of acetone. The flask containing the fluoborate suspension was rinsed with 20 mL of acetone, and the rinse was added to the reaction mixture. Upon completion of addition which required 7 minutes, the reaction mixture was stirred for about 18 hours. The reaction mixture was filtered to collect 2.0 grams of 6-chloro-2-[ethoxy(thiocarbonyl)thio]benzoic acid. The nmr spectrum was consistent with the proposed structure.

후처리

  1. additionwas added, by pipette
  2. washwas rinsed with 20 mL of acetone
  3. additionthe rinse was added to the reaction mixture
  4. additionUpon completion of addition which required 7 minutes
  5. filtrationThe reaction mixture was filtered
  6. customto collect 2.0 grams of 6-chloro-2-[ethoxy(thiocarbonyl)thio]benzoic acid

출처 및 근거

ORD 기록
ord-e4a02d485eee4678bd9bd9ba28dd128f
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05149357

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