Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183096Generated: November 1, 2026

Methanol → 3-Phenyl-5-(phenylmethoxy)-1H-indazole

https://huagongshe.com/reaction/2183096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantStannous ChlorideHCID 24479—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 57440914HCID 57440914—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Phenyl-5-(phenylmethoxy)-1H-indazoleHCID 2247992548%

Reaction Steps

To a solution of 2-amino-5-(phenylmethoxy)phenyl phenyl ketone (2.6 g, 8.0 mmol) in 6N HCl (70 mL) at 0° C. was added a solution of sodium nitrite (NaNO2) (650 mg, 9.4 mmol) in water (2 mL). To this solution was added methanol and THF to keep it homogeneous. A solution of tin (II) chloride (SnCl2) (5.3 g, 23.6 mmol) in concentrated HCl (20 mL) was then added. The solution was stirred at room temperature overnight. The solid was then filtered and the solution concentrated and chromatographed on silica gel eluting with 20% ethyl acetate in hexane to give the title compound (1.15 g, 48% yield). 1H NMR (DMSO-d6) δ 13.1 (s, 1H), 7.95 (d, 2H), 7.56-7.48 (m, 6H), 7.44-7.3 (m, 4H), 7.14 (d, 1H), 5.12 (s, 2H); ES-MS (m/z) 301 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-af765a917b5c440fab3383442516c9af
Source noteuspto-grants-2005_05