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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914847Generated: October 31, 2026

Triphenylphosphine → HCID 22248248, compound

https://huagongshe.com/reaction/914847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2-FluorothiophenolHCID 520216—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22248248HCID 222482485%

Reaction Steps

After dissolving 1.97 g of 2-fluorothiophenol in 50 ml of tetrahydrofuran, 3.0 g of 1-(tert-butoxycarbonyl)piperidine-4-methanol and 4.03 g of triphenylphosphine were added, and then 3.3 ml of diethyl azodicarboxylate was added dropwise while cooling on ice and the mixture was stirred overnight at room temperature. The reaction solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (216 mg, 5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265108B2
Source datasetuspto-grants-2007_09
ORD IDord-b58131ec73e8461286e2b33a3a408d8f
Source noteuspto-grants-2007_09