Hydrogen Sulfide → HCID 178496264, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][C:7](Cl)=[O:8].C(N(CC)CC)C.[SH2:17]>C(Cl)Cl>[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][C:7]([OH:8])=[S:17]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-methoxyethoxyacetyl chloride (700 mg.; 4.59 mmoles) in methylene chloride (10 ml.; dried over molecular sieves) was added dropwise at 0°-5° to a stirred solution of triethylamine (0.7 ml.; 508 mg.; 5.04 mmoles) in methylene chloride (20 ml.) which had been saturated at 0°-5° with H2S (ca. 30 min.). The light yellow mixture was stirred at 0°-5° for 30 min. and then at room temperature for 30 min. The mixture was washed with 1N HCl (10 ml.×2) and then brine. The CH2Cl2 layer was dried (Na2SO4) and evaporated yielding 2-methoxyethoxythioacetic acid (480 mg.; 3.20 mmoles; yield 69.7%) as a light yellow liquid: nmr (CDCl3): δppm 3.42 (3H, s, --OCH3), 3.4-3.9 (4H, m, --CH2CH2 -), 4.10 (2H, s, -OCCH2O), 5.0 (1H, br, -COSH); ir (neat): 2550 cm-1 (νS-H), 1770 (νc=o, thio acid).
Workup
- waitat room temperature for 30 min
- washThe mixture was washed with 1N HCl (10 ml.×2)
- dry with materialThe CH2Cl2 layer was dried (Na2SO4)
- customevaporated
Sources & evidence
- ORD record
- ord-30579d51eec248f0a54f9b417d79227f
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04182711
Reaction notes
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