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Thioglycolic Acid → 2-(2,5-Dichlorophenyl)-2-mercaptoacetic acid

HRID 248600
Notes
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Reaction equation

HRID 248600 reaction equation
Br[C:2]1[C:3]([Cl:9])=[C:4](Cl)[CH:5]=[CH:6][CH:7]=1.[Cl:10]C1C(Cl)=C(Cl)C=CC=1.[C:19]([OH:23])(=[O:22])[CH2:20][SH:21].[OH-].[K+]>>[Cl:9][C:3]1[CH:4]=[CH:5][C:6]([Cl:10])=[CH:7][C:2]=1[CH:20]([SH:21])[C:19]([OH:23])=[O:22]
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 1133Thioglycolic AcidHCID 68951,2,3-TrichlorobenzeneHCID 14797Potassium HydroxideHCID 420661-Bromo-2,3-dichlorobenzene

Product 1

HCID 224923292-(2,5-Dichlorophenyl)-2-mercaptoacetic acid

Procedure

Using the combinations of monobromodichlorobenzene or trichlorobenzene, thioglycolic acid, potassium hydroxide and solvent listed in Table 2, the reaction was carried out in the same manner as in Example 8 or 9 to yield 2,5-dichlorophenylthioglycolic acid. The results are given in Table 2.

Sources & evidence

ORD record
ord-635a18898f7e475884fece1683af069a
Source dataset
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05210291

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes