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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469366Generated: October 29, 2026

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

https://huagongshe.com/reaction/469366

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-chloropyrimidine-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 numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-04090373bc6546358ffa2a2306c3b493
Source noteuspto-grants-2014_01