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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293844Generated: November 1, 2026

Carbon tetrabromide → HCID 21471327, compound

https://huagongshe.com/reaction/2293844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 11109137HCID 11109137—
SolventDichloromethaneHCID 6344—
SolventChlorineHCID 24526—
ProductHCID 21471327HCID 21471327—

Reaction Steps

A solution of carbon tetrabromide (2.958 gm, 8.92 mmol) in CH2 Cl2 (10 ml) was added over a 15 minute period to a cold (-10° C.) solution of 2-(4-fluorophenyl)-4-(1-methylethyl)-3-quinolinecarboxaldehyde (1.744 gm, 5.95 mmol) (the preparation of which is described in Example 2) and triphenylphosphine (4.680 gm, 17.84 mmol) in CH2Cl2 (34 ml). After the addition was complete, the mixture was stirred for 20 minutes then quenched with saturated NaHCO3 and extracted 3× with CH2Cl2. The combined organic layers were washed with brine, dried (Na2SO4), filtered and stripped to give a yellow-orange oil. The oil was chromatographed (flash, Merck SiO2, 30% CH2 Cl2 in hexane followed by 1:1 CH2Cl2 in hexane followed by straight CH2Cl2) to give 3-(2,2-dibromoethenyl)-2-(4-fluorophenyl)-4-(1-methylethyl)quinoline as a colorless foam (2.572 gm,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686433
Source datasetuspto-grants-1997_11
ORD IDord-49d881b661324d578f7401dd32d106ad
Source noteuspto-grants-1997_11