Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661995Generated: October 28, 2026

Benzyl Alcohol → 5-(Benzyloxy)-6-bromo-1H-indazole

https://huagongshe.com/reaction/1661995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant6-Bromo-1H-indazol-5-olHCID 59159946—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-(Benzyloxy)-6-bromo-1H-indazoleHCID 6676704970.2%

Reaction Steps

To a solution of 6-bromo-5-hydroxy-1H-indazole (5 g, 23.5 mmol) in THF (50 mL) is added benzyl alcohol (3.05 g, 28.2 mmol), PPh3 (7.39 g, 28.2 mmol) and diethylazodicarboxylate (4.46 mL, 28.2 mmol). After the reaction mixture is stirred at RT overnight, EtOAc (50 mL) and saturated aqueous NH4Cl (30 mL) are added. The organic phase is separated, dried over MgSO4, and concentrated. The residue is purified by silica gel column chromatography eluting with PE:EtOAc (4:1) to provide the product (5.0 g, 70.2% yield). MS (m/z): 303.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-808a9cc82f2145129a401af8e37a52d8
Source noteuspto-grants-2011_10