Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221223Generated: November 1, 2026

Hexane → HCID 10158332, compound

https://huagongshe.com/reaction/2221223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 22032966HCID 22032966—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10158332HCID 1015833264.3%

Reaction Steps

[1-Benzyl-7-(3-chloro-4-fluorophenyl)-1H-indol-3-yl](oxo)acetic acid was prepared from ethyl 2-[1-benzyl-7-(3-chloro-4-fluorophenyl)-1H-indol-3-yl]-2-oxoacetate (0.139 g, 0.319 mmol), and potassium hydroxide (0.076 g, 1.35 mmol) in THF (2.5 mL) and water (2.5 mL) following the procedure described in Step 4 of Example 5. Following work-up, and trituration of the residue with hexane, a solid was obtained. Drying for 12 hours at 82° C. yielded the title compound as a yellow solid (0.0836 g, 64%), mp: 153-156° C. Mass spectrum (−ESI, [M−H]−) m/z 406; 1HNMR (500 MHz, DMSO-d6): δ 13.8-14.2 (br s, 1H), 8.65 (s, 1H), 8.35 (m, 1H), 7.3-7.35 (m, 2H), 7.05-7.2 (m, 5H), 7.0 (s, 1H, J=7.1 Hz), 6.35 (d, 2H, J=6.9 Hz), 5.35 (d, 1H, J=16.6 Hz), and 5.15 ppm (d, 1H, J=16.6 Hz). Elemental Analysis for C23H15ClFNO3: Calculated: C, 67.74; H, 3.71; N, 3.43. Found: C, 67.53; H, 3.9; N, 3.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-2b5dd283b3d2490bb2f41f0761ee3ae8
Source noteuspto-grants-2008_05