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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047987Generated: October 31, 2026

Potassium Carbonate → Methyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyanochroman-4-carboxylate

https://huagongshe.com/reaction/1047987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-chlorophenethyl)-4-hydroxybenzamideHCID 60628097—
ReactantMethyl 6-cyano-7-fluorochroman-4-carboxylateHCID 67080208—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyanochroman-4-carboxylateHCID 6708026448.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

Methyl 6-cyano-7-fluorochroman-4-carboxylate (50 mg, 0.21 mmol) was diluted with 1-methyl-2-pyrrolidinone (2 mL) followed by the addition of K2CO3 (147 mg, 1.1 mmol) and N-(4-chlorophenethyl)-4-hydroxybenzamide (59 mg, 0.21 mmol). The reaction was bubbled with argon for 10 minutes and then heated to 110° C. and stirred for 6 hours. After the reaction was allowed to cool, it was loaded directly onto a Biotage 25 column and eluted with 5% ethyl acetate/hexanes to 100% ethyl acetate to yield methyl 7-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-6-cyanochroman-4-carboxylate (50 mg, 48% yield). MS (ESI)=490.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569522B2
Source datasetuspto-grants-2013_10
ORD IDord-d762d2f26d5a49d3bc878854622be6c4
Source noteuspto-grants-2013_10