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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173393Generated: October 30, 2026

Ethyl orthoformate → HCID 67517645, compound

https://huagongshe.com/reaction/2173393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
ReactantHCID 12404389HCID 12404389—
SolventAcetic AcidHCID 176—
ProductHCID 67517645HCID 67517645—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of (4-amino-2-bromophenyl)acetic acid (230 mg, 1 mmol) and triethyl orthoformate (444 mg, 3 mmol) in 8 mL of HOAc was added sodium azide (80 mg, 1.2 mmol), and the mixture was heated to 100° C. for 3 hours. The reaction mixture was cooled to ambient temperature and the solvent was removed under vacuum. The residue was dissolved in EtOAc, washed with water, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by prep-TLC to afford [2-bromo-4-(1H-tetrazol-1-yl)phenyl]acetic acid. 1H-NMR (300 MHz, MeOD) δ ppm 9.78 (s, 1H), 8.16 (s, 1H), 7.83˜7.87 (m, 1H), 7.60˜7.63 (m, 1H), 3.89 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-1d45739b775d4e0fadb359af5d83fc15
Source noteuspto-grants-2015_06