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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854976Generated: October 30, 2026

Sodium Hydroxide → HCID 11196915, compound

https://huagongshe.com/reaction/854976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69517330HCID 69517330—
SolventEthanolHCID 702—
ProductHCID 11196915HCID 11196915—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of ethyl 6-ethyl-8-methyl-2- (trifluoromethyl)-2H-chromene-3-carboxylate (2.6 g, 8.3 mmol) in EtOH (90 mL), was added IN NaOH (24.8 mL, 24.8 mmol). The reaction was stirred at 25° C. for 18 h. The ethanol was removed from the reaction under reduced pressure. The residue was acidified with 2N HCl. The product was extracted into EtOAc (300 mL) then washed with brine (100 mL), dried over MgSO4, filtered, and concentrated. The crude product was dissolved in 20 mL EtOAc and then diluted with 150 mL hexane. The resulting solution was chilled at 0° C. for 30 min. The product, which precipitated from the solution, was collected by filtration. The desired product was isolated as an off-white solid in quantities of 1.6 g (68%). 1H NMR (DMSO-d6) 1.15 (t, 3H, J=7.56 Hz), 2.16 (s, 3H), 2.51 (q, 2H, J=7.6 Hz), 5.89 (q, 1H, J=7.4 Hz), 7.11 (d, 1H, J=2.1 Hz), 7.14 (d, 1H, J=2.1 Hz), 7.79 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-27b4f637b8e144ab9aa52e9bb532aad8
Source noteuspto-grants-2007_08