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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253146Generated: October 25, 2026

Water → Benzyl 4-(2-(4-propyl-1H-1,2,3-triazol-1-yl)acetyl)morpholine-2-carboxylate

https://huagongshe.com/reaction/253146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-PentyneHCID 12309—
ReactantSodium AscorbateHCID 23667548—
ReactantBenzyl 4-(2-azidoacetyl)morpholine-2-carboxylateHCID 86614022—
CatalystCopper sulfate pentahydrateHCID 24463—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-(2-(4-propyl-1H-1,2,3-triazol-1-yl)acetyl)morpholine-2-carboxylateHCID 66845266875%

Reaction Steps

In a sealable vessel, benzyl 4-(2-azidoacetyl)morpholine-2-carboxylate (0.096 g, 0.32 mmol) was suspended in t-BuOH (1 mL) and water (1 mL) was added. An aqueous solution of sodium ascorbate (1.0 M, 0.032 ml, 0.032 mmol) and an aqueous solution of copper(II) sulfate pentahydrate (0.30 M, 0.079 ml, 0.024 mmol) were added, followed by pent-1-yne (0.040 ml, 0.41 mmol). The vessel was sealed and placed in a 65 deg oil bath, whereupon the mixture was stirred for 14 h. The reaction mixture was cooled to RT, taken up in EtOAc (60 mL), and the organic layer was extracted with dilute sodium bicarbonate (5 mL), dilute brine (5 mL), and saturated brine (5 mL), then was dried over sodium sulfate and concentrated. The residue was purified through silica gel (25 mL) eluting with EtOAc, affording the title compound (105 mg, 0.28 mmol). MS m/z 373 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-faeb4f8a57de4cb992633bfb8d63a567
Source noteuspto-grants-2011_01