Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Decylamine | HCID 8916 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Acetyloxy)-4-(methylsulfanyl)butanoic acid | HCID 3074728 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86689978 | HCID 86689978 | — |
Reaction Steps
To a solution of 2-acetoxy-4-(methylthio)butanoic acid (17.1 g, 89 mmol) in dichloromethane (350 mL) at 0° C. was added thionyl chloride (32.4 mL, 445 mmol) dropwise over 1 hr. The reaction was stirred at 0° C. for 1.5 hrs then the cooling bath was removed and the reaction was warmed to room temperature with stirring for 3 hrs. The solvent was evaporated and the resulting oil was dried under high vacuum for 1 hr to give an orange oil. A solution of the resulting oil in dichloromethane (˜30 mL) was added to a solution of triethylamine (24.8 mL, 178 mmol) and decylamine (17.8 mL, 89 mmol) in dichloromethane (150 mL) at 0° C. and the reaction was allowed to warm to room temperature with stirring overnight. The reaction was evaporated, redissolved in EtOAc (300 mL) and washed with 1N HCl (3×150 mL), saturated sodium bicarbonate (3×150 mL), and brine(1×150 mL). The organic layer was dried over magnesium sulfate, filtered and evaporated to give an oil. The oil was purified by silica gel chromatography with 0-40% EtOAc/heptane to give a yellow oil. (21.1 g, 71%). m/z 332 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169203B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-723a906ca81847aca2932a0580490096 |
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| Source note | uspto-grants-2015_10 |
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