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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393318Generated: October 29, 2026

Sodium Hydroxide → HCID 12018480, compound

https://huagongshe.com/reaction/393318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21883689HCID 21883689—
SolventEthanol tetrahydrofuran waterHCID 18504229—
ProductHCID 12018480HCID 1201848060.1%

Reaction Steps

Aqueous NaOH (1.31 mL, 3.277 mmol, 2.5 M solution) was added in one portion to the ester (Step 1) (0.880 g, 2.731 mmol) in THF:EtOH:H2O (7:2:1, 10 mL). The resulting solution was stirred for 60 hours. The reaction mixture was partially concentrated in vacuo to remove the organic solvents and was diluted with H2O. The resulting aqueous solution was washed with diethyl ether, sparged with nitrogen to remove trace ether, and acidified with concentrated HCl. The resulting oily suspension was extracted with diethyl ether. The combined organic phases were dried over MgSO4, filtered and concentrated in vacuo yielding the title compound (0.483 g, 60%) as an oil which solidified as a white crystalline mass: mp 134.7-136.2° C. 1H NMR (acetone-d6/300 MHz) 7.97 (s, 1H), 7.73 (s, 1H), 7.67 (dd, 1H, J=8.5, 1.0 Hz), 7.17 (d, 1H, J=8.5 Hz), 6.89 (t, 1H, J=56.2 Hz), 5.90 (q, 1H, J=7.1 Hz). FAB-ESLRMS m/z 293 (M−H). EIHRMS m/z 293.0235 (M−H, Calc'd 293.0237). Anal. Calc'd for C12H7F5O3: C, 49.00; H, 2.40. Found: C, 48.78; H, 2.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806288B1
Source datasetuspto-grants-2004_10
ORD IDord-91ad02470363403cbafaf261a0f599a2
Source noteuspto-grants-2004_10