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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108854Generated: November 3, 2026

Water → HCID 57629444, compound

https://huagongshe.com/reaction/2108854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant5-(5-Bromopentyloxy)-2-(hydroxymethyl)-4H-pyran-4-oneHCID 17975837—
ReactantHCID 178469560HCID 178469560—
SolventDimethylformamideHCID 6228—
ProductHCID 57629444HCID 5762944431%

Reaction Steps

4-Hydroxy-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester (0.86 g, 3.02 mmol) was dissolved in DMF (10 mL). Cs2CO3 (0.98 g, 3.02 mmol) was added at RT and the mixture was stirred for 10 min. A solution of 5-(5-bromo-pentyloxy)-2-hydroxymethyl-pyran-4-one 10 (0.86 g, 3.02 mmol) in DMF (5 mL) was added via syringe. This mixture was stirred at 50° C. for 22 h. Water (10 mL) was added and the mixture extracted with EtOAc (2×50 mL), washed with water (3×50 mL), brine (3×50 mL) dried over MgSO4, filtered and evaporated. The crude product was purified by column chromatography on silica using as eluent (CH2Cl2:MeOH)=90:10. 4-[5-(6-Hydroxymethyl-4-oxo-4H-pyran-3-yloxy)-pentyloxy]-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester 13 was obtained (0.43 g, 31% yield) as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514432B2
Source datasetuspto-grants-2009_04
ORD IDord-a07bd55c87614e92be1e5d24a5f4608d
Source noteuspto-grants-2009_04