Thioglycolic Acid → HCID 54468475, compound
Reaction equation
[CH:1]([C:5]1[CH:13]=[CH:12][C:8]2[O:9][CH2:10][O:11][C:7]=2[CH:6]=1)=[CH:2][CH2:3][CH3:4].[SH:14][CH2:15][C:16]([OH:18])=[O:17]>C(OCC)(=O)C>[O:9]1[C:8]2[CH:12]=[CH:13][C:5]([CH2:1][CH:2]([S:14][CH2:15][C:16]([OH:18])=[O:17])[CH2:3][CH3:4])=[CH:6][C:7]=2[O:11][CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.2 g of 5-(1-butenyl)-1,3-benzodioxole and 5.4 g of mercaptoacetic acid were heated at 60° C. for 3 h. The reaction mixture was diluted with ethyl acetate, washed with water and an aqueous common salt solution and dried over magnesium sulfate. The solvent was distilled off and the product was separated according to silica gel column chromatography (chloroform) to obtain 1.8 g of the intended compound in the form of a colorless oil.
Workup
- washwashed with water
- dry with materialan aqueous common salt solution and dried over magnesium sulfate
- distillationThe solvent was distilled off
- customthe product was separated
Sources & evidence
- ORD record
- ord-14484b7157b448bd88300314c6b7fcc5
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05110956
Reaction notes
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