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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490855Generated: October 27, 2026

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

https://huagongshe.com/reaction/490855

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, I=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 numberUS07528176B2
Source datasetuspto-grants-2009_05
ORD IDord-f2505e8950b24c6d8d33be1cc40a5d5b
Source noteuspto-grants-2009_05