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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096365Generated: October 31, 2026

Water → (6-Chloro-pyrimidin-4-yl)-(7-methyl-2,3-dihydro-benzofuran-5-yl)-methanone

https://huagongshe.com/reaction/2096365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-Chloropyrimidine-4-carbonyl chlorideHCID 18422098—
Reactant7-Methyl-2,3-dihydrobenzofuranHCID 22592386—
SolventDichloromethaneHCID 6344—
Product(6-Chloro-pyrimidin-4-yl)-(7-methyl-2,3-dihydro-benzofuran-5-yl)-methanoneHCID 58181093—

Reaction Steps

0.396 g (2.24 mmol) 6-chloropyrimidin-4-carboxylic acid chloride and 0.328 g (2.46 mmol) aluminium trichloride in 10 mL DCM were stirred for 20 min at RT. Then 0.300 g (2.24 mmol) 7-methyl-2,3-dihydro-benzofuran in DCM were added dropwise to the reaction mixture and this was stirred for 1.5 h at RT. After the addition of water and DCM to the reaction mixture the phases were separated and the aqueous phase was extracted with DCM. The combined organic phases were washed with saturated aqueous sodium hydrogen carbonate solution, dried on sodium sulphate, filtered and evaporated down i.vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450327B2
Source datasetuspto-grants-2013_05
ORD IDord-786c5ffffc684b228a777d55fc09e09e
Source noteuspto-grants-2013_05