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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501772Generated: October 29, 2026

Hydrochloric Acid → HCID 23021543, compound

https://huagongshe.com/reaction/501772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 68458090HCID 68458090—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 23021543HCID 2302154345.1%

Reaction Steps

0.98 g of methyl 4-{[4-[4-(cyclopentyloxy)-2-hydroxybenzoyl]-2-(3-methoxy-3-oxopropyl)phenoxy]methyl}-2-methoxybenzoate was dissolved in a mixed solvent of 10 mL of methanol and 10 mL of tetrahydrofuran, to which 2 mL of a 20% aqueous solution of sodium hydroxide was added at room temperature, and then this mixture was stirred for one hour at the same temperature. The reaction mixture to which water was added was adjusted to pH 2 with 6M hydrochloric acid, followed by the addition of ethyl acetate thereto, and the organic phase was separated therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, this washed phase was dried over anhydrous magnesium sulfate and the solvent was distilled out under reduced pressure. The resultant residue was recrystallized from ethanol to yield 0.42 g of 4-({2-(2-carboxyethyl)-4-[4-(cyclopentyloxy)-2-hydroxybenzoyl]phenoxy}methyl)-2-methoxybenzoic acid as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772285B2
Source datasetuspto-grants-2010_08
ORD IDord-ef7cd289bb5740f29c0cdcbf6aa85454
Source noteuspto-grants-2010_08