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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021370Generated: November 1, 2026

Methanol → 7-(4-((4-Chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylic acid

https://huagongshe.com/reaction/1021370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylateHCID 67080218—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-(4-((4-Chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylic acidHCID 6708042330.9%

Reaction Steps

Methyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyano-2,2-dimethylchroman-4-carboxylate (2.0 mg, 0.00385 mmol) was diluted with THF (500 μL) followed by the addition of NaOH (0.00771 mL, 0.0385 mmol) and 200 μL of water and methanol. After stirring for 3 hours, the reaction was diluted with ethyl acetate and 2N HCl. The layers were separated and the organic layer was dried over MgSO4, filtered and concentrated. The material was purified using a 0.5 mm preparative TLC plate, eluting with 5% methanol/0.5% acetic acid/CH2Cl2 to yield the title compound (0.6 mg, 30.8% yield) as a white solid. MS (ESI)=504.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-3598b875ce0940c584a5e054f5e89b78
Source noteuspto-grants-2014_05