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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269871Generated: October 30, 2026

Triphenylphosphine → 1-(t-Butoxycarbonyl)-4-(1-(2-fur-2-ylmethoxy-ethyl)-1h-benzimidazole-2-carbonyl)piperidine

https://huagongshe.com/reaction/2269871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantFur-2-ylmethyl 2-hydroxyethyl etherHCID 10103270—
Reactant1-(t-butoxycarbonyl)-4-(1H-benzimidazole-2-carbonyl)piperidineHCID 18333235—
SolventTetrahydrofuranHCID 8028—
SolventPropan-2-one--dichloromethane (1/1)HCID 21584124—
Product1-(t-Butoxycarbonyl)-4-(1-(2-fur-2-ylmethoxy-ethyl)-1h-benzimidazole-2-carbonyl)piperidineHCID 18333465—

Reaction Steps

Combine 1-(t-butoxycarbonyl)-4-(1 H-benzoimidazole-2-carbonyl)-piperidine (1.71 g, 5.2 mmol), fur-2-ylmethyl 2-hydroxyethyl ether (0.74 g, 5.2 mmol), and triphenylphosphine (0.31.67 g, 6.4 mmol) in tetrahydrofuran (20 mL). Add diethyl azodicarboxylate (1.0 mL, 6.35 mmol). After 21 hours, evaporate the reaction mixture in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 5% acetone/dichloromethane to give 1-(t-butoxycarbonyl)-4-(1-(2-fur-2-ylmethoxy-ethyl)-1 H-benzoimidazole-2-carbonyl)-piperidine: Rf=0.30 (silica gel, 5% acetone/dichloromethane)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329392B1
Source datasetuspto-grants-2001_12
ORD IDord-c7bb4817aea244d9a708f61fcf7e0d36
Source noteuspto-grants-2001_12