Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | (S)-methyl-2-hexylthiodecanoate | HCID 18656172 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178443479 | HCID 178443479 | 90% |
Reaction Steps
To a 12 L flask equipped with a condenser and overhead stirrer was added (S)-methyl-2-hexylthiodecanoate (302.5 g, 1.00 mol), and 3 L of dry acetonitrile. To this solution was added sodium iodide (600 g, 4.00 mol) and iodine (25.4 g, 0.10 mol) followed by chlorotrimethylsilane (543 g, 635 ml, 5.00 mol). The reaction was heated to an internal temperature of 55° C. After 12 hours, an additional portion of chlorotrimethylsilane (130 g, 152 mL, 1.20 mol) was added and heating continued for 8 hours. The reaction was cooled to 0° C., 6 L of hexane was added followed by 1 L of ice water, and the layers were allowed to separate. The top hexane layer was separated and set aside. The combined CH3CN/water layers were extracted with hexane (2×6 L). The combined hexane layers were washed with 1 L of water, 0.1M Na2S2O3 (2×3 L) and once with 3 L of 1:1 brine/water. The combined hexane extracts were dried with MgSO4, filtered and concentrated to give (S)-2-hexylthiodecanoic acid (260 g, 0.90 mol, 90%) a colorless oil: [α]D =-59.40° (C=1, MeOH); 1H NMR δ3.19 (m, 1H), 2.63 (m, 2H), 1.95-1.18 (m, 22H), 0.95 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05498786 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-c7f31bf238fc45f2bc3ac24235d93d10 |
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| Source note | uspto-grants-1996_03 |
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