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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064755Generated: November 1, 2026

Iodine → HCID 11175139, compound

https://huagongshe.com/reaction/1064755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
Reactant1-(4'-Hydroxy-1,1'-biphenyl-3-yl)ethanoneHCID 11218106—
SolventAmmoniaHCID 222—
SolventWaterHCID 962—
ProductHCID 11175139HCID 1117513921%

Reaction Steps

The product from Example 136A (5.76 g, 27 mmol) was suspended in concentrated aqueous ammonia (400 mL) and treated with a solution of potassium iodide (23.3 g, 140 mmol) and iodine (7.24 g, 28.5 mmol) in water (100 mL). As the reaction did not go to completion, the mixture was treated with a second solution of potassium iodide (15.8 g, 95 mmol) and iodine (4.83 g, 19 mmol) in water (50 mL). After an hour the ammonia was removed under reduced pressure on a rotary evaporator. The mixture was extracted with EtOAc, and the combined organic phases were washed consecutively with pH 6 potassium phosphate buffer and brine, then dried (Na2SO4), concentrated, and chromatographed through silica with 1% acetic acid in a gradient of 0 to 5% EtOAc/CH2Cl2 to provide the title compound as a beige powder (21% yield). MS (ESI APCI negative ion detection) m/z 337 (M−H)−; 1HNMR (300 MHz, CDCl3) δ 2.65 (s, 3 H), 5.37 (bs, 1 H), 7.08 (d, 1 H), 7.48-7.55 (m, 2 H), 7.71 (ddd, 1 H), 7.88-7.93 (m, 2 H), 8.09 (dd, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-e1525197e9e24935bf92fb7d452f01db
Source noteuspto-grants-2005_11