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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630841Generated: October 31, 2026

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

https://huagongshe.com/reaction/1630841

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 numberUS08791141B2
Source datasetuspto-grants-2014_07
ORD IDord-10bf6151ea084a629dfd14bcbd75d7a7
Source noteuspto-grants-2014_07