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Thioglycolic Acid → HCID 20348735、化合物

HRID 1701155
ノート
印刷プレビュー

反応式

HRID 1701155 の反応式
[SH:1][CH2:2][C:3]([OH:5])=[O:4].[OH-].[K+].[F:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:20]=[CH:19][C:18]([CH:21](Cl)[CH3:22])=[CH:17][CH:16]=1.C1(C)C=CC=CC=1>CO.O>[F:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:16]=[CH:17][C:18]([CH:21]([S:1][CH2:2][C:3]([OH:5])=[O:4])[CH3:22])=[CH:19][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 1133Thioglycolic AcidHCID 1140TolueneHCID 14797Potassium HydroxideHCID 203487834'-(1-Chloroethyl)-2-fluoro-1,1'-biphenyl

生成物 1

HCID 20348735HCID 20348735、化合物収率 55%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 962
Water
溶媒
2 回

実験手順

6.35 gm (0.055 mol) of 80% mercaptoacetic acid were admixed in 70 ml of methanol with a solution of 6.2 gm (0.11 mol) of potassium hydroxide in 6.2 ml of water. To the solution of dipotassium salt, 11.7 gm (0.05 mol) of 1-(2'-fluoro-4-biphenylyl)-1-chloro-ethane were added, the reaction mixture was rinsed with 20 ml of methanol and stirred for 18 hours at room temperature. Subsequently, the mixture was evaporated, the residue was digested with acetone, and the precipitated potassium salt was suction-filtered off. The free acid was obtained by dissolving the salt in water and acidifying the solution. M.p 128°-130° C. (from toluene). Yield: 55% of theory.

後処理

  1. washthe reaction mixture was rinsed with 20 ml of methanol
  2. customSubsequently, the mixture was evaporated
  3. filtrationthe precipitated potassium salt was suction-filtered off
  4. customThe free acid was obtained

出典と根拠

ORDレコード
ord-84eb262934c24fdab5d2cb07f93fb5d2
出典データセット
uspto-grants-1980_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04191776

反応ノート

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