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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042015Generated: October 30, 2026

Borane;tetrahydrofuran → 4-(5-Oxazolyl)benzylamine

https://huagongshe.com/reaction/2042015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant4-(5-Oxazolyl)-benzamideHCID 21930999—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Oxazolyl)benzylamineHCID 2193099332.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 4-(5-oxazolyl)benzamide (500 mg, 2.657 mmol) in 10 mL of dry THF was cooled to 0° C. and 10 mL of 1 M BH3.THF (10.00 mmol) was added. The contents were refluxed overnight and the excess borane was destroyed by dropwise addition of methanol. The solvent was evaporated and the residue was treated with methanolic HCl to decompose the amine-borane complex. After evaporation of the methanol, the residue was taken in water, basified to pH 10 and the product was extracted in to DCM. The DCM layer was dried (K2CO3) and the solvent was removed to provide 150 mg (32%) of 4-(5-oxazolyl)benzylamine: 1H NMR (CDCl3) δ 7.90 (s, 1H), 7.60 (d, 2H), 7.40 (d, 2H), 7.30 (s, 1H), 3.90 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586576B2
Source datasetuspto-grants-2013_11
ORD IDord-0600f35303fb4dd3bf44dda8544e8ac6
Source noteuspto-grants-2013_11