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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174523Generated: October 30, 2026

Hydrochloric Acid → HCID 118108336, compound

https://huagongshe.com/reaction/2174523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-PropanolHCID 1031—
Reactant5-Methoxyindole-2-carboxylic acidHCID 20401—
ProductHCID 118108336HCID 11810833688%

Reaction Steps

To a suspension of 300 (670 mg, 3.50 mmol) in anhydrous n-PrOH (20 mL) was added HCl (4 N in dioxane, 2.5 mL). The reaction mixture was heated at reflux for 36 h. Upon completion, volatiles were evaporated in vacuo and the resulting oil was purified by chromatography (0% to 20% EtOAc/hexanes) to produce a white powder (721 mg, 88%): mp 104-107° C. TLC Rf 0.51 (20% EtOAc/hexanes). 1H NMR (600 MHz, CDCl3) δ 8.82 (s, 1H), 7.32-7.31 (d, 1H, J=8.94 Hz), 7.15 (m, 1H), 7.08 (d, 1H, J=2.4 Hz), 7.01-6.99 (dd, 1H, J1=8.94 Hz, J2=2.46 Hz), 4.32-4.29 (t, 2H, J=6.72 Hz), 3.85 (s, 3H), 1.84-1.78 (sex, 2H, J=7.38 Hz), 1.05-1.03 (t, 3H, J=7.38 Hz). 13C NMR (150 MHz, CDCl3) δ 162.0, 154.7, 132.1, 127.88, 127.85, 117.0, 112.7, 108.2, 102.5, 66.5, 55.7, 22.2, 10.5. Elemental analysis calculated for C13H15NO3: C, 66.94; H, 6.48; N, 6.00. Found: C, 66.87; H, 6.44; N; 6.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061994B1
Source datasetuspto-grants-2015_06
ORD IDord-b88a6022a3a4434ca3ccbc8b95a98012
Source noteuspto-grants-2015_06