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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809161Generated: October 30, 2026

Acetic Acid → HCID 57312355, compound

https://huagongshe.com/reaction/1809161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant3-AminobenzamideHCID 1645—
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 57312355HCID 5731235580%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a round bottom flask was added 3-aminobenzamide (1.36 g, 10.0 mmol, 1.0 eq.), acetic acid (9.1 mL, 160 mmol, 16.0 eq.), triethyl orthoformate (5.4 mL, 32.0 mmol, 3.2 eq.), and sodium azide (0.812 g, 12.5 mmol, 1.25 eq.). The reaction mixture was then heated to 80° C. until all solids were dissolved. The reaction was stirred at 80° C. for an additional 2 h before cooling to RT. Water (6.0 mL,) was added, followed by 6N HCl (5.3 mL), and then 25% NaNO2 (2.1 mL). The resulting precipitate was filtered and rinsed with water to give pure tetrazole 38 (1.5 g, 80% yield). LC/MSD (HP Series 1100 MSD) MS (ES+) m/z 189.9 (M+H)+1, 187.9 (M−H)+1 1H-NMR, Varian 400 MHz (DMSO-d6) δ 10.1 (s, 1H), 8.39 (t, 1H), 8.20 (br. s, 1H), 8.05 (m, 2H), 7.72 (t, 1H), 7.55 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362017B2
Source datasetuspto-grants-2013_01
ORD IDord-f863b46ed13f48d0b3d429146887c40d
Source noteuspto-grants-2013_01