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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639536Generated: November 2, 2026

Ammonium Chloride → HCID 178525021, compound

https://huagongshe.com/reaction/1639536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantBenzyl 2-benzyloxy-5-cyanobenzoateHCID 18974028—
SolventDimethylformamideHCID 6228—
ProductHCID 178525021HCID 178525021101.9%

Reaction Steps

A solution of 436 mg (1.27 mmol) of benzyl 2-benzyloxy-5-cyanobenzoate, 91 mg (1.40 mmol) of sodium azide, and 68 mg (1.27 mmol) of ammonium chloride in 5 mL of DMF is heated at 120° C. for 24 hrs. The DMF was removed by rotoevaporation, the residue is taken up in water, and acidified. The white precipitate is collected by filtration and dried to give 500 mg of unpurified benzyl 2-benzyloxy-5-(1H-tetrazol-5-yl)benzoate, which is treated with 28% aqueous ammonium hydroxide in 5 mL of MeOH at 85° C. for 72 hrs. The reaction mixture was concentrated, taken up in water, and then acidified. Filtration of the precipitate gives 400 mg (1.04 mmol, 82% yield) of 2-benzyloxy-5-(1H-tetrazol-5-yl)benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110570B2
Source datasetuspto-grants-2012_02
ORD IDord-dc3f10dcd0af4f3da12dd460bb2199b3
Source noteuspto-grants-2012_02