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Ethyl xanthate → HCID 19876591、化合物

HRID 1885977
ノート
印刷プレビュー

反応式

HRID 1885977 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8823Ethyl xanthateHCID 26255TetrafluoroborateHCID 5462222PotassiumHCID 15059421HCID 15059421、化合物

生成物 1

HCID 19876591HCID 19876591、化合物

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e4a02d485eee4678bd9bd9ba28dd128f
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05149357

反応ノート

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