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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626388Generated: October 30, 2026

Potassium Carbonate → tert-Butyl 7-(4-carbamoylphenoxy)-6-cyanochroman-4-carboxylate

https://huagongshe.com/reaction/1626388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzamideHCID 65052—
ReactantTert-butyl 6-cyano-7-fluorochroman-4-carboxylateHCID 67288243—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Producttert-Butyl 7-(4-carbamoylphenoxy)-6-cyanochroman-4-carboxylateHCID 8666439183.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

tert-butyl 6-cyano-7-fluorochroman-4-carboxylate (290 mg, 1.05 mmol), 4-hydroxybenzamide (172 mg, 1.25 mmol) and potassium carbonate (347 mg, 2.51 mmol) were diluted with dry NMP (4 mL). The reaction was bubbled with argon for 10 minutes and then heated at 120° C. for 12 hours under a slight argon bubble. The reaction was cooled and loaded directly onto a biotage 40 M cartridge, eluting with 20% ethyl acetate/hexanes to 100% ethyl acetate to yield 1 g of the crude product which was found to contain NMP. The residue was taken up in ethyl acetate and washed twice with water and then brine. The organic layer was dried over magnesium sulfate, filtered and concentrated to provide the desired product (343 mg, 83.2% yield) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785445B2
Source datasetuspto-grants-2014_07
ORD IDord-7e69ab0e696b4935b8d04bf867f93f50
Source noteuspto-grants-2014_07