Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268701Generated: October 30, 2026

Potassium Carbonate → Tert-butyl-7-[(2-(4-bromophenyl)-5-methyl-1,3-oxazol-4-yl)methoxy]chromane-3-carboxylate

https://huagongshe.com/reaction/268701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Bromophenyl)-4-(chloromethyl)-5-methyloxazoleHCID 10957108—
ReactantTert-butyl 7-hydroxychromane-3-carboxylateHCID 59832111—
SolventWaterHCID 962—
ProductTert-butyl-7-[(2-(4-bromophenyl)-5-methyl-1,3-oxazol-4-yl)methoxy]chromane-3-carboxylateHCID 6927960877.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred suspension of tert-butyl 7-hydroxychromane-3-carboxylate (1.1 g, 4.4 mmol) and potassium carbonate (1.1 g, 8 mmol), 2-(4-bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole (1.14 g, 4 mmol) was added and the reaction mixture was stirred at 60° C. for overnight. After the completion of the reaction, water (40 ml) was added and the precipitated product was extracted with ethylacetate (60 ml). The organic layer was washed with 50 ml of water twice and dried. The dried solution was evaporated to give the product as brown solid (1.55 g, 77.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446127B2
Source datasetuspto-grants-2008_11
ORD IDord-a3d340ab3ed64250b45df0e7cea8363c
Source noteuspto-grants-2008_11