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Thioglycolic Acid → HCID 20348735, 화합물

HRID 1701155
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HRID 1701155 반응식
[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
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참가 물질

7

반응물 4

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

생성물 1

HCID 20348735HCID 20348735, 화합물수율 55%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매
2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-84eb262934c24fdab5d2cb07f93fb5d2
출처 데이터셋
uspto-grants-1980_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04191776

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