Potassium Carbonate → (2,2-Diethoxyethyl)(3-methoxyphenyl)sulfane
Reaction equation
[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5]Br)[CH3:2].[CH3:10][O:11][C:12]1[CH:13]=[C:14]([SH:18])[CH:15]=[CH:16][CH:17]=1.C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[CH2:1]([O:3][CH:4]([O:7][CH2:8][CH3:9])[CH2:5][S:18][C:14]1[CH:15]=[CH:16][CH:17]=[C:12]([O:11][CH3:10])[CH:13]=1)[CH3:2]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Bromoacetaldehyde diethyl acetal (16.5 ml, 0.11 mol) was added dropwise to a mixture of m-methoxybenzenethiol (15.0 ml, 0.12 mol) and K2CO3 (16.6 g, 0.12 mol) in acetone (150 ml) at room temperature. The reaction mixture was stirred for 16 hours and then filtered. The solid was washed with acetone, and the combined filtrate and washes were concentrated in vacuo. The residue was diluted with H2O and extracted with Et2O. The Et2O extracts were washed with 0.5M KOH, H2O, and brine, dried over Na2SO4, filtered, and concentrated in vacuo to give 27.4 g of 1-[(2,2-diethoxy)ethylthio]-3-methoxybenzene as a dark yellow oil. 'H NMR, δ: (CDCl3): 1.18 (6H, t, --OCH2CH3); 3.13 (2H, d, --SCH--); 3.43--3.73 (4H, m, --OCH2CH3); 3.77 (3H, s, -- OCH3); 4.67 (1H, t, --SCH2CH--); 6.60-7.27 (4H, m, aromatics).
Workup
- filtrationfiltered
- washThe solid was washed with acetone
- concentrationthe combined filtrate and washes were concentrated in vacuo
- additionThe residue was diluted with H2O
- extractionextracted with Et2O
- washThe Et2O extracts were washed with 0.5M KOH, H2O, and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-3a846eae33d14bc5937d718d85c626c8
- Source dataset
- uspto-grants-1988_11
- Patent number
- US04788192
Reaction notes
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