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ChemicalBook CAS DataBase List 2,3-Dihydro-5-methyl-4H-1-benzopyran-4-one

2,3-Dihydro-5-methyl-4H-1-benzopyran-4-one synthesis

5synthesis methods
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Yield:18385-68-7 45% ,18385-69-8 55%

Reaction Conditions:

with acid activated montmorillonite K-10 in toluene; for 0.5 h;Reflux;Inert atmosphere;

Steps:

General experimental procedure for the synthesis of chroman-4-one (4a-4p)

General procedure: A mixture of 3-aryloxypropionic acid 3a-3o (1.0 mmol) and freshly prepared AA.Mont.K-10 (300% by weight) in toluene (2 mL) was heated to reflux under inert atmosphere for the specified time (30-45 minutes). After reaction completion, reaction mixture is cooled and added CH2Cl2 (10-15 mL). Filtered the AA.Mont.K-10 and washed twice with CH2Cl2. The organic filtrate is concentrated and the crude mass is extracted with hexane (10-15 mL) to afford pure chromanones 4a-4p.

References:

Begum, Ayisha F.;Balasubramanian, Kalpattu K.;Shanmugasundaram, Bhagavathy [Tetrahedron Letters,2021,vol. 82,art. no. 153372] Location in patent:supporting information