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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406681Generated: November 2, 2026

tert-Butanol → HCID 86681378, compound

https://huagongshe.com/reaction/1406681

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantBenzyl azideHCID 12152—
ReactantSodium AscorbateHCID 23667548—
Reactant5-Ethynyl-2-hydroxybenzaldehydeHCID 45083574—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
ProductHCID 86681378HCID 8668137850%

Reaction Steps

5-ethynylsalicylaldehyde (2{26}, 50 mg, 0.34 mmol, 1.0 equiv.) and benzyl azide (91 mg, 86 μL, 0.68 mmol, 2.0 equiv.) were suspended in 1:1 t-BuOH:H2O (1.2 mL). Sodium L-ascorbate (24 mg in 100 μL H2O, 0.34 mmol, 1.0 equiv.) was added, followed by copper (II) sulfate pentahydrate (67 mg in 200 μL H2O, 0.10 mmol, 0.33 equiv.). The reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with H2O (10 mL), and the aqueous layer was extracted with DCM (3×10 mL). The combined organic layers were washed with brine (10 mL), dried over Mg504, filtered, and concentrated. The crude product was purified by silica gel column chromatography (25-50% EtOAc/hexanes) to yield 2{27} (47.5 mg, 0.17 mmol, 50.0%) as an off-white solid. 1H-NMR (500 MHz, CDCl3): δ 11.03 (s, 1H), 9.92 (s, 1H), 8.07 (d, 1H, J=2.5 Hz), 7.86 (dd, 1H, J=2.0, 8.0 Hz), 7.65 (s, 1H), 7.41-7.35 (m, 3H), 7.31 (dd, 2H, J=2.0, 7.5 Hz), 7.01 (d, 1H, J=8.5 Hz), 5.57 (s, 2H). 13C-NMR (125 MHz, CDCl3): δ 196.5, 161.3, 134.4, 134.2, 130.6, 129.1, 128.8, 128.1, 124.9, 122.9, 120.6, 118.9, 118.1, 54.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916705B2
Source datasetuspto-grants-2014_12
ORD IDord-3535624e74574f99b1bf74c87900e8ad
Source noteuspto-grants-2014_12