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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408323Generated: October 27, 2026

1,4-Dibromobutane → 3-(4-Bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-triene

https://huagongshe.com/reaction/2408323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
Reactant3-Bromobicyclo[4.2.0]octa-1,3,5-trieneHCID 10866980—
ReactantHCID 178418306HCID 178418306—
Product3-(4-Bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-trieneHCID 58028492—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a clean and dry 1000 ml round bottom flask equipped with a 250 ml addition funnel, low temperature thermometer and magnetic stir bar was transferred anhydrous tetrahydrofuran (500.0 ml) under nitrogen. 4-bromobenzocyclobutane (25.0 g, 0.1370 mol) was added to this flask by syringe. The reaction vessel was placed into a dry ice/acetone bath until a temperature of <−70° C. was achieved. The reaction mixture was then allowed to stir for 45 minutes at a stirring speed of 550 rpm in order to verify the integrity of the stirring apparatus at this temperature. Tert-butyllithium solution (161 ml, 0.2730 mol) was transferred to the addition funnel by cannula, then added dropwise to the reaction never allowing the temperature to rise above −65° C. Following addition, the reaction was allowed to stir for a period of 30 minutes. The vessel was then removed from the dry ice/acetone bath and allowed to warm to a temperature of −20° C. The vessel was then again placed into the dry ice/acetone bath until a temperature of <−70° was achieved. 1,4-dibromobutane (64.7 ml, 0.5460 mol) was added to the reaction dropwise via syringe, maintaining the current temperature. The reaction was allowed to stir for 30 minutes at this temperature following addition. The reaction was slowly warmed to room temperature over the following 12 hours. Reaction completion was confirmed by GC-MS. After warming, the reaction was quenched by the addition of isopropanol (25.0 ml) via syringe.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815639B2
Source datasetuspto-grants-2014_08
ORD IDord-b98e08f1c06d4043bedec7b7196bf316
Source noteuspto-grants-2014_08