Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10219842 | HCID 10219842 | — |
Reaction Steps
Dimethyl phosphite (11.0 g 0.1 mol) was added dropwise to a stirred solution of 2.4 g (0.1 mole) of sodium hydride in 50 mL of dry THF at 25-30° C. under N2. The mixture was stirred under reflux until H2 evolution ceased. It was then cooled to 6° C. and was added with stirring to carbon disulfide (38 g, 0.5 mol) at 2-8° C. over 15 min. Methyl iodide (14.2 g 0.1 mol) was then added at 5° C. over 15 min. The mixture was quenched with 350 mL of ice-water and extracted with ether (100 mL×3). The ether layers were combined, dried with anhydrous magnesium sulfate, filtered, evaporated to remove ether and distilled in vacuo. The fraction boiling between 92-94° C./50μ was collected, 6.5 g, Y=32.5%. (Put footnote 2 here) 1H NMR: δ(ppm) 3.85 (d, 6H, 3JHP=10 Hz, POCH3), 2.69 (d, 3H, JHP=1 Hz CSCH3); 13C NMR: δ(ppm) 228(d, 1JCP=175 Hz, CS), 54.5 (d, 2JCP=6 Hz, POCH3), 10.9 (s, CSCH3); 31P NMR {H}: δ(ppm) 0.30(s); 31P NMR: δ(ppm) 0.30 (m, 3JPH=11 Hz); HRMS: 199.9732 (Found); 199.9731 (Calcd).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444837B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-7a60eb3f85494e68a2a4add30e948b3d |
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| Source note | uspto-grants-2002_09 |
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