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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108640Generated: October 30, 2026

Iodine → HCID 86603460, compound

https://huagongshe.com/reaction/2108640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
ReactantHCID 25150022HCID 25150022—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventMethylamineHCID 6329—
ProductHCID 86603460HCID 86603460—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 3,5-dimethyl-4-(4′-methoxymethoxy-3′-iso-propylbenzyl)phenol (1.0 g, 3.18 mmol, Chiellini et al., Bioorg. Med. Chem. Lett. 10:2607 (2000)) in C2H5OH (30.0 mL) and 40% aqueous methylamine (6.20 mL) at 0° C. was added a solution of potassium iodide (2.5 g, 15.0 mmol) and iodine (0.98 g, 3.82 mmol) in H2O (6.20 mL). The reaction mixture was stirred at 0° C. for 1 h, quenched with water and extracted with ethyl acetate (2×30 mL). The organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with 20% ethyl acetate in hexanes to afford 3,5-dimethyl-2-iodo-4-(4′-methoxymethoxy-3′-iso-propylbenzyl)phenol as white solid: 1H NMR (300 MHz, CD3OD): δ 6.93 (m, 2 H), 6.65 (m, 2 H), 5.18 (s, 2 H), 4.05 (s, 2 H), 3.48 (s, 3 H), 3.30 (m, 1 H), 2.41 (s, 3 H), 2.19 (s, 3 H), 1.18 (d, J=6.6 Hz, 6 H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=ethyl acetate-hexanes (1:5); Rf=0.60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514419B2
Source datasetuspto-grants-2009_04
ORD IDord-85f6c0e7633c4f69b4404592925ac9bc
Source noteuspto-grants-2009_04