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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720728Generated: November 1, 2026

Carbon tetrabromide → HCID 15099566, compound

https://huagongshe.com/reaction/1720728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 21471506HCID 21471506—
SolventDichloromethaneHCID 6344—
ProductHCID 15099566HCID 1509956699%

Reaction Steps

A solution of carbon tetrabromide (2.866 gm, 8.64 mmol) in CH2Cl2 (8 ml) was added over a 10 minute period to a cold (-10° C.) solution of 2-(4-Fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinecarboxaldehyde (1.840 gm, 5.76 mmol) (the preparation of which is described in Example 3) and triphenylphosphine (4.590 gm, 17.5 mmol) in CH2Cl2 (30 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 2× with CH2Cl2. The combined organic layers were washed with saturated NaHCO3, dried (Na2SO4), filtered and concentrated. The concentrate was chromatographed (flash, Merck, SiO2, 1:1 CH2Cl2 : hexane) to give 3-(2,2-Dibromoethenyl)-2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenylpyridine as a white solid (2.701 gm, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506219
Source datasetuspto-grants-1996_04
ORD IDord-d92a42577fd14c42af492605061cc413
Source noteuspto-grants-1996_04