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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628756Generated: October 29, 2026

Water → 4-Iodo-1-chloro-2-[[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]methyl]benzene

https://huagongshe.com/reaction/628756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPhenol, 4-((2-chloro-5-iodophenyl)methyl)-HCID 86698895—
ReactantTert-butyldimethylsilane chlorideHCID 131722836—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-Iodo-1-chloro-2-[[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]methyl]benzeneHCID 12388870288.2%

Reaction Steps

4-(2-chloro-5-iodobenzyl)phenol (8.5 g, 24.7 mmol) and triethylamine (5.0 g, 49.5 mmol) were dissolved in methylene chloride (200 mL). To the resulting mixture were added tert-butyldimethylsilane chloride (5.6 g, 37.1 mmol) and 4-(dimethylamino)pyridine (305 mg, 2.5 mmol) at 0° C. After the completion of addition, the mixture was warmed up to room temperature, and stirred for 18 hr. To the mixture was added water (100 mL). The resulting mixture was separated into an aqueous phase and an organic phase. The aqueous phase was extracted with methylene chloride (100 mL×2). The organic phases were combined, washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulphate, and concentrated under a reduced pressure. The resulting crude product was purified with a silica-gel column chromatography (ethyl acetate:petroleum ether=0-1:100) to produce 10.0 g of a product in a yield of 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315438B2
Source datasetuspto-grants-2016_04
ORD IDord-9864721d8e6e4c6092ae3013880570c7
Source noteuspto-grants-2016_04