Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425279Generated: October 28, 2026

2-Bromothiophene → 1-(5-Bromothiophen-2-YL)heptan-1-one

https://huagongshe.com/reaction/2425279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiopheneHCID 13851—
ReactantHeptanoyl chlorideHCID 17313—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
Product1-(5-Bromothiophen-2-YL)heptan-1-oneHCID 57675566—

Reaction Steps

2-Bromothiophene (1.63 g, 10.0 mmol) and heptanoyl chloride (1.78 g, 12.0 mmol) were dissolved in dry benzene (15 mL) and AlCl3 was added in portions with stirring over 10 min. The resulting dark brown solution was refluxed for 1 hr and left to cool down to room temperature. The mixture was quenched with 2M HCl (15 mL) carefully while stirred. The organic layer was separated, washed with 2M HCl, 2M NaOH, and water, and passed through silica column (d=3 cm, l=8 cm). The solution was dried over MgSO4, and concentrated in vacuo (2.40 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964650B2
Source datasetuspto-grants-2011_06
ORD IDord-efaadd103a804e22b2752b045e0defc9
Source noteuspto-grants-2011_06