Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040447Generated: November 1, 2026

Ammonium Chloride → HCID 178521700, compound

https://huagongshe.com/reaction/1040447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantHCID 57916539HCID 57916539—
SolventDimethylformamideHCID 6228—
ProductHCID 178521700HCID 17852170063.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a round bottom flask was added (1-cyano-cyclopropyl)-carbamic acid benzyl ester (500 mg, 2.31 mmol) in DMF (4 ml), followed by the addition of NaN3 (195 mg, 3 mmol) and NH4Cl (161 mg, 3 mmol). The reaction mixture was stirred at 110° C. for 24 h. The reaction mixture was concentrated in vacuo. The residue was dissolved in EtOAc/water. The organic layer was separated, washed with brine, dried under any. Na2SO4, filtered and concentrated to afford 380 mg of [1-(1H-tetrazol-5-yl)-cyclopropyl]-carbamic acid benzyl ester as a off-white solid, m/z 260.8 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552205B2
Source datasetuspto-grants-2013_10
ORD IDord-d154f3c93fab4cff9c8d3146c84c67c7
Source noteuspto-grants-2013_10