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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710244Generated: October 29, 2026

1-Azido-4-fluorobenzene → (S)-tert-Butyl 2-(4-(1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)phenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/710244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Azido-4-fluorobenzeneHCID 10887974—
Reactant(S)-tert-butyl 2-(4-ethynylphenyl)morpholine-4-carboxylateHCID 89689402—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiisopropylethylamineHCID 81531—
Product(S)-tert-Butyl 2-(4-(1-(4-fluorophenyl)-1H-1,2,3-triazol-4-yl)phenyl)morpholine-4-carboxylateHCID 11841298228.4%

Reaction Steps

1-Azido-4-fluorobenzene (24 mg, 0.174 mmol) was dissolved in N,N-diisopropylethylamine (0.75 ml), then (S)-tert-butyl 2-(4-ethynylphenyl)morpholine-4-carboxylate (50 mg, 0.175 mmol) was added followed by copper(I) iodide (33 mg, 0.174 mmol). The mixture was stirred at room temperature for 3 h. The green mixture was concentrated on the rotavap, silica gel (0.5 g) was added and after short grinding the mixture was put on a silica gel column for purification. Flash chromatography (5 g silica gel, 30% ethyl acetate in heptane) yielded a white solid (21 mg, 28%). MS (ISP): 369.1 ([M-tBu+H]+), 425.2 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181230B2
Source datasetuspto-grants-2015_11
ORD IDord-60a29c3938d6495ba2ccafdd9d507156
Source noteuspto-grants-2015_11