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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440515Generated: November 2, 2026

Iodine → HCID 178443479, compound

https://huagongshe.com/reaction/1440515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(S)-methyl-2-hexylthiodecanoateHCID 18656172—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
ProductHCID 178443479HCID 17844347990%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498786
Source datasetuspto-grants-1996_03
ORD IDord-c7f31bf238fc45f2bc3ac24235d93d10
Source noteuspto-grants-1996_03