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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905478Generated: November 1, 2026

2,4,6-Trimethylpyridine → HCID 54049138, compound

https://huagongshe.com/reaction/1905478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantPhosphorus tribromideHCID 24614—
ReactantLithium BromideHCID 82050—
Reactant4-Cyanophenylethyl cyclopropyl carbinolHCID 13316971—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 54049138HCID 54049138130.7%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 9.8 g of 4-cyanophenylethyl cyclopropyl carbinol in 140 ml of ether was added 4.24 g of lithium bromide and 3 ml of 2,4,6-collidine. The mixture was cooled to -60° C. and 9.8 g of phosphorus tribromide was added over a five minute period. The reaction mixture was allowed to warm to 0° C., kept at that temperature for two hours and then allowed to warm to 18° C. Collidine (18 ml) was added, and after 15 minutes of stirring, the mixture was poured into 200 ml of water and 100 ml of ether. The ether extracts were washed with dilute aqueous sulfuric acid and water, dried over anhydrous magnesium sulfate and concentrated to a volume of 150 ml. Zinc bromide (11.6 g) was then added with cooling, and the mixture was stirred at room temperature for 29 hours. The ether solution was washed with water, dried and concentrated to give 12.5 g of 4-(6-bromohex-3-enyl)benzonitrile as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843087
Source datasetuspto-grants-1989_06
ORD IDord-68c7a5f96c994699ac4d9bc81ccb00f4
Source noteuspto-grants-1989_06