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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928592Generated: October 26, 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/1928592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidomethyl 2,2-dimethylpropanoateHCID 11521126—
ReactantSodium AscorbateHCID 23667548—
Reactant5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridineHCID 57708431—
Reactant2-Methylpropan-2-ol--water (1/1)HCID 71401949—
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 tert-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 numberUS08183381B2
Source datasetuspto-grants-2012_05
ORD IDord-ab95be482abf409eac2209d7effad6cd
Source noteuspto-grants-2012_05