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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507986Generated: November 2, 2026

Pyridine → HCID 23157610, compound

https://huagongshe.com/reaction/507986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromineHCID 24408—
ReactantHCID 23157476HCID 23157476—
SolventDichloromethaneHCID 6344—
ProductHCID 23157610HCID 23157610102.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 1-(2-ethoxyethoxy)-2,3,5-trimethylbenzene (1.0 g, 4.08 mmol), pyridine (0.097 mL, 1.20 mmol) and dichloromethane (10 mL) was added a solution of bromine (0.66 g, 4.12 mmol) in dichloromethane (1 mL) under stirring at 0° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=49/1-hexane/ethyl acetate=4/1) to give the title compound (1.2 g, yield 99%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-dfe7e953381c423e9ff913c9dbfe42d3
Source noteuspto-grants-2010_08