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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495051Generated: November 1, 2026

Water → HCID 10760196, compound

https://huagongshe.com/reaction/495051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHCID 11382904HCID 11382904—
ReactantHCID 131722467HCID 131722467—
SolventAcetonitrileHCID 6342—
ProductHCID 10760196HCID 1076019661%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a flame dried flask was added iodolactone (8) (0.33 g, 0.90 mmol) followed by dry acetonitrile (12 mL). Sodium iodide (0.22 g, 1.44 mmol) was added followed by chlorotrimethylsilane (0.18 mL, 1.44 mmol). The resulting mixture was stirred at 22° C. for 15 minutes at which point H2O (7.6 μL, 0.42 mmol) was added and the mixture was heated at 60° C. After 5 hours at 60° C. the mixture was poured into a 1:1 solution of 50 Na2SO3/Brine (75 mL) and then quickly extracted with EtOAc (6×75 mL). The organic layer was dried (MgSO4) and chromatographed (CH2Cl2:MeOH 95:5) to yield iodopyridone (9) as a white solid 0.19 g (61%): 1H NMR (300 MHz, CDCl3/CD3OD) δ 0.62 (t, J=7 Hz, 3 H), 1.45-1.54 (m, J=7 Hz, 2 H), 2.80 (d, J=14 Hz, 1 H), 2.97 (d, J=14 Hz, 1 H), 4.93 (d, J=15 Hz, 1 H), 5.06 (d, J=15 Hz, 1 H), 6.66 (s, 1 H); 13C NMR (75 MHz, CDCl3) δ 7.5, 35.6, 41.9, 61.6, 72.5, 94.4, 118.3, 121.1, 156.5, 162.6, 172.7; HRMS (EI) m/z calcd for C11H12INO4 (M+) 348.9811, found 348.9815 LRMS (EI) m/z 349 (M+), 331, 320, 303, 289, 278, 264, 250, 162, 150, 122, 94, 57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538220B2
Source datasetuspto-grants-2009_05
ORD IDord-8f7fb0b1e3bc415e85ec64ad98be5af4
Source noteuspto-grants-2009_05