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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661615Generated: October 30, 2026

Carbon tetrabromide → 3-(2,2-Dibromo-vinyl)-4-methoxy-pyridine

https://huagongshe.com/reaction/1661615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Formyl-4-methoxypyridineHCID 11332503—
SolventDichloromethaneHCID 6344—
Product3-(2,2-Dibromo-vinyl)-4-methoxy-pyridineHCID 58215548—

Reaction Conditions

Temperature0 °C

Reaction Steps

A flask is charged with triphenylphosphine (21.4 g, 81.6 mmol), carbon tetrabromide (13.5 g, 40.8 mmol) and dichloromethane (300 mL). 4-Methoxy-pyridine-3-carbaldehyde (2.8 g, 20.4 mmol) in dichloromethane (300 mL) is added at 0° C. The mixture is stirred at 0° C. for 1 h. The mixture is extracted with saturated aqueous ammonium chloride and the aqueous phase is neutralized with NaHCO3 and extracted with dichloromethane. The organic phase is dried over Na2SO4, concentrated and purified by silica gel chromatography eluting with a 0 to 10% methanol-dichloromethane gradient to give 3-(2,2-dibromo-vinyl)-4-methoxy-pyridine. 1H NMR (400 MHz, CDCl3) δ ppm 3.90 (s, 3H), 6.81 (d, J=5.8 Hz, 1H), 7.48 (s, 1H), 8.48 (d, J=5.8 Hz, 1H), 8.76 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-a363e24c299f4fa08d0ca6a5875340a7
Source noteuspto-grants-2011_10