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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434141Generated: November 1, 2026

Hydrochloric Acid → HCID 23087471, compound

https://huagongshe.com/reaction/1434141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57934373HCID 57934373—
ReactantHCID 66627175HCID 66627175—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23087471HCID 2308747194.6%

Reaction Steps

Synthesized from N-ethyl-4-hydroxy-N-[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]benzamide and ethyl chloroacetate according to an analogous synthetic method to Preparation Example 40, to a solution of the resulting {4-{ethyl[5-methoxy-2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)phenyl]carbamoyl}phenoxy}acetic acid ethyl ester (275 mg) in tetrahydrofuran (5 ml) was added an aqueous solution of 1N sodium hydroxide (5 ml) on an ice bath. The solution was stirred for 1.5 hours while warming to room temperature, then the reaction solution was acidified with 2N hydrochloric acid on the ice bath. Water was added thereto, the solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, then the solvent was evaporated in vacuo to provide the title compound (246 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-6bc67d04375640c585e57231b1fbdfb6
Source noteuspto-grants-2009_11