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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221241Generated: October 30, 2026

Potassium Hydroxide → (1-Benzyl-5-phenyl-1H-indol-3-yl)(oxo)acetic Acid

https://huagongshe.com/reaction/2221241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactantethyl {1-benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetateHCID 22032978—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzyl-5-phenyl-1H-indol-3-yl)(oxo)acetic AcidHCID 1029173262.3%

Reaction Steps

{1-Benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetic acid was prepared from ethyl {1-benzyl-5-phenyl-1H-indol-3-yl}(oxo)acetate (0.680 g, 1.77 mmol), and potassium hydroxide (0.322 g, 5.74 mmol) in THF (10 mL) and water (10 mL), following the procedure described in Step 4 of Example 5. Crystallization from acetonitrile, and drying for 3.5 hours at 70° C., yielded the title compound as a yellow solid (0.392 g, 62%), mp: 193-195° C. (dec.). Mass spectrum (+ES, [M+H]+) m/z 356; 1HNMR (500 MHz, DMSO-d6): δ 13.7-14.2 (br s, 1H), 8.7 (s, 1H), 8.45 (d, 1H, J=0.61 Hz), 7.65 (m, 3H), 7.55 (dd, 1H, J=8.7 Hz and 1.1 Hz), 7.45 (t, 2H, J=7.6 Hz), 7.25-7.35 (m, 6H), and 5.65 ppm (s, 2H). Elemental Analysis for C23H17NO3: Calculated: C, 77.73; H, 4.82; N, 3.94. Found: C, 77.52; H, 4.81; N, 3.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-d7c588a6ca83453ebe51913dd22d4759
Source noteuspto-grants-2008_05