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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80641Generated: October 25, 2026

Azidomethyl 2,2-dimethylpropanoate → (4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate

https://huagongshe.com/reaction/80641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidomethyl 2,2-dimethylpropanoateHCID 11521126—
ReactantWater butanolHCID 22253497—
ReactantSodium AscorbateHCID 23667548—
Reactant5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridineHCID 57708431—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product(4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalateHCID 57708433—

Reaction Steps

To a solution of azidomethyl pivalate (4.26 g, 27.1 mmol) in 1:1 text -butanol water (90 mL total) was added 5-(prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine (5.45 g, 27.1 mmol), sodium ascorbate (1.4 mL of a 1M solution in water) and copper sulfate (1.4 mL of a 1M solution in water). The solution was stirred at room temperature for 72 hours. Water was added and the suspension was extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to afford the expected product which was used in the next step without further purification. 1H NMR (DMSO-d6): δ 10.07 (1H, s), 8.43-8.41 (2H, m), 8.00 (1H, d, J=8.8 Hz), 7.88 (1H, dd, J=3.2, 8.8 Hz), 6.32 (2H, s), 5.38 (2H, s), 1.08 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846675B2
Source datasetuspto-grants-2014_09
ORD IDord-6cb9a023f229469fa1e8821c6da6f32f
Source noteuspto-grants-2014_09