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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359244Generated: October 29, 2026

Potassium Hydroxide → HCID 10142554, compound

https://huagongshe.com/reaction/1359244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 69831236HCID 69831236—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10142554HCID 1014255488.5%

Reaction Steps

Following the procedure described in Step 4 of Example 6, [1-bromo-6-(5-chloro-3-pentanoyl-benzofuran -2-yl)-naphthalen-2-yloxy]-acetic acid ethyl ester (0.25 g, 0.46 mmol) was hydrolyzed with potassium hydroxide (0.300 g, 5.36 mmol) in THF (10 mL) and water (10 mL). Crystallization from ethyl acetate afforded the title compound as an off-white solid (0.21 g), mp 130-132° C. Mass spectrum (−APCl, [M−H]−) m/z 513, 515, 517. 1HNMR (400 MHz, DMSO-d6): δ13.25 (br s,1H), 8.48 (d,1H, J=1.5 Hz), 8.25 (d, 1H, J=9.0 Hz), 8.14 (d, 1H, J=9.0 Hz), 8.04 (d, 1H, J=2.2 Hz), 7.99 (dd, 1H, J=9.0, 1.8 Hz), 7.79 (d, 1H, J=8.8 Hz), 7.52-7.48 (m, 2H), 5.03 (s, 2H), 2.72 (t, 2H, J=7.3 Hz), 1.56-1.48 (m, 2H), 13H, 1.17-1.07 (m, 2H), and 0.70 ppm (t, 3H, J=7.4 Hz). Elemental Analysis for C25H20BrClO5: Calculated: C, 58.22; H, 3.91; N, 0.00. Found: C, 58.24; H, 3.73; N, 0.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599925B2
Source datasetuspto-grants-2003_07
ORD IDord-cdb77e4abda14cb1badb5a5840d19453
Source noteuspto-grants-2003_07