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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850474Generated: October 30, 2026

Pyridine → HCID 19363467, compound

https://huagongshe.com/reaction/850474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantValeryl chlorideHCID 61186—
ReactantHCID 19363524HCID 19363524—
SolventWaterHCID 962—
ProductHCID 19363467HCID 19363467400%

Reaction Steps

4-Amino-3-pentyloxybenzoic acid (200 mg, 0.90 mmol), methylene chloride (5 ml) and pyridine (0.081 ml, 1.0 mmol) were mixed, and valeryl chloride (0.11 ml, 0.90 mmol) was added to this solution. The mixture was stirred at room temperature for 0.5 hour. Water was added to the reaction mixture, and the aqueous layer was extracted 3 times with ethyl acetate (5 ml). The organic layers were combined, washed with saturated brine (10 ml), and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate was concentrated under reduced pressure. The obtained crude crystals were washed with hexane to give 4-pentanoylamino-3-pentyloxybenzoic acid (109.5 mg, 400%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-f0f6dec37b6744daae4e17009bbb223c
Source noteuspto-grants-2000_01