Methyl Thioglycolate → HCID 19828252, compound
Reaction equation
[CH2:1]([O:9][N:10]1[C:15]([CH3:17])([CH3:16])[CH2:14][CH:13]([OH:18])[CH2:12][C:11]1([CH3:20])[CH3:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:21](OC)(=[O:24])[CH2:22][SH:23].[NH2-].[Li+]>C1(C)C=CC=CC=1>[C:21]([O:18][CH:13]1[CH2:14][C:15]([CH3:17])([CH3:16])[N:10]([O:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[C:11]([CH3:19])([CH3:20])[CH2:12]1)(=[O:24])[CH2:22][SH:23]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The general procedure of Example 1 is followed using 2.09 grams (7.0 mmol) of 1-octyloxy-4-hydroxy-2,2,6,6-tetramethylpiperidine, 0.74 gram (7.0 mmol) of methyl thioglycolate and 0.17 gram of lithium amide in 50 ml of toluene to afford the title compound after purification by silica gel chromatography.
Sources & evidence
- ORD record
- ord-171fc11990b641149d2146fa52b16df9
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05026750
Reaction notes
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