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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297536Generated: October 30, 2026

Water → 4-(3-Iodostyryl)phenol

https://huagongshe.com/reaction/1297536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron tribromideHCID 25134—
Reactant(E)-1-iodo-3-[2-(4-methoxyphenyl)ethenyl]benzeneHCID 11013106—
SolventDichloromethaneHCID 6344—
Product4-(3-Iodostyryl)phenolHCID 1091423492%

Reaction Steps

To a solution of 8 (350 mg, 1.00 mmol) in CH2Cl2 (200 mL) was added BBr3 (10 mL, 1M in hexane) dropwise at −78° C. in a dry ice-acetone bath. The mixture was allowed to warm up to room temperature. Water was added while the reaction mixture was cooled at 0° C. in an ice bath. The mixture was extracted with CH2Cl2. The organic phase was dried and filtered. The filtrate was purified by flash chromatography (EtOAc: Hex, 1:9) to give 9 (296 mg, 92%). 1H NMR (200 MHz, CDCl3): δ 4.81 (s, 1H), 6.83 (d, J=16.17 Hz, 1H), 6.84 (m, 2H), 7.03 (d, J=16.32 Hz, 1H), 7.06 (t, J=7.8 Hz, 1H), 7.36–7.57 (m, 4H), 7.84 (s, 1H); 13C NMR (50 MHz, CDCl3): δ 94.75, 115.67, 124.96, 125.49, 128.09, 129.48, 129.87, 130.25, 135.01, 135.96, 139.90, 155.53; HRMS: m/z Calcd for C14H11IO: 321.9855; Found: 321.9840.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250525B2
Source datasetuspto-grants-2007_07
ORD IDord-adb7058c1d3e43ed8cf41ff964039ec3
Source noteuspto-grants-2007_07