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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272735Generated: November 2, 2026

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

https://huagongshe.com/reaction/1272735

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 numberUS07208513B2
Source datasetuspto-grants-2007_04
ORD IDord-6db48e02de604b849ce1a0d6aaea7abc
Source noteuspto-grants-2007_04