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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508473Generated: November 1, 2026

Iodine → HCID 123511408, compound

https://huagongshe.com/reaction/1508473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl 2-(5-methoxy-2,3-dihydro-1H-inden-1-yl)acetateHCID 10263432—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 123511408HCID 123511408—

Reaction Steps

Ethyl (5-methoxy-2,3-dihydro-1H-inden-1-yl)acetate (472 mg, 2.015 mmol) was dissolved in ethanol (20 mL). Iodine (511 mg, 2.015 mmol) and silver sulfate (628 mg, 2.015 mmol) were added and the reaction was stirred vigorously at room temperature, protected from light, for 1 hour. The reaction was diluted with ethyl acetate (75 mL) and filtered to remove solids. The filtrate was washed with sodium bisulfite (2×50 mL), water (70 mL), and brine (70 mL). The organic layer was dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash chromatography on silica gel with 0 to 50% ethyl acetate/hexanes. Further purification by SFC on a chiral AD column with 15% IPA/heptanes removed a minor regioisomer and separated the two enantiomers of ethyl (6-iodo-5-methoxy-2,3-dihydro-1H-inden-1-yl)acetate. 1H NMR (CDCl3, 500 MHz) δ 7.55 (s, 1H), 6.72 (s, 1H), 4.17 (m, 2H), 3.85 (s, 3H), 3.53 (m, 1H), 2.95-2.65 (m, 3H), 2.60-2.42 (m, 2H), 1.78 (m, 1H), 1.28 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221834B2
Source datasetuspto-grants-2015_12
ORD IDord-e1c922229d0940068b3508d1e2fd2b07
Source noteuspto-grants-2015_12