Potassium Carbonate → (2,2-Diethoxyethyl)(3-methoxyphenyl)sulfane

HRID 2232338Notes

Reaction equation

HRID 2232338 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

5

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

  1. filtrationfiltered
  2. washThe solid was washed with acetone
  3. concentrationthe combined filtrate and washes were concentrated in vacuo
  4. additionThe residue was diluted with H2O
  5. extractionextracted with Et2O
  6. washThe Et2O extracts were washed with 0.5M KOH, H2O, and brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-3a846eae33d14bc5937d718d85c626c8
Source dataset
uspto-grants-1988_11
Patent number
US04788192

Reaction notes

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