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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293839Generated: October 29, 2026

Carbon tetrabromide → HCID 14621980, compound

https://huagongshe.com/reaction/2293839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 14621979HCID 14621979—
SolventDichloromethaneHCID 6344—
SolventChlorineHCID 24526—
ProductHCID 14621980HCID 14621980102.2%

Reaction Steps

A solution of carbon tetrabromide (2,204 gm, 6.65 mmol) in CH2 Cl2 (8 ml) was added over a 12 minute period to a cold (-12° C.) solution of 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinecarboxaldehyde (1.415 gm, 4.43 mmol) (the preparation of which is described in Example 1) and triphenylphosphine (3,488 gm, 13.3 mmol) in CH2Cl2 (25 ml). After the addition was complete, the cooling bath was removed and the mixture was stirred for 20 minutes. The solution was quenched with saturated NaHCO3 and extracted 3× with CH2Cl2. The combined organic layers were washed with saturated NaHCO3, dried (Na2SO4), filtered and stripped to give a yellow oil. The oil was chromatographed (flash, Merck SiO2, 40% CH2Cl2 in hexane) to give 3-(2,2-dibromoethenyl)-4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenylpyridine as a colorless foam (2.152 gm, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686433
Source datasetuspto-grants-1997_11
ORD IDord-e799fc325e844d5b94dd6d0a4b5f84c9
Source noteuspto-grants-1997_11