Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(2-Methoxyethoxy)acetyl chloride | HCID 7010338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178496264 | HCID 178496264 | 69.7% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182711 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-30579d51eec248f0a54f9b417d79227f |
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| Source note | uspto-grants-1980_01 |
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