Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401136Generated: October 29, 2026

Tributylphosphine → N-Boc-3-(2-piperidin-4-yl-ethoxy)-benzoic acid ethyl ester

https://huagongshe.com/reaction/1401136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
SolventTetrahydrofuranHCID 8028—
ProductN-Boc-3-(2-piperidin-4-yl-ethoxy)-benzoic acid ethyl esterHCID 6693005497.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

N-Boc-4-piperidine ethanol (15 g, 65 mmol) and ethyl 3-hydroxybenzoate (11 g, 65 mmol) were dissolved in dry THF (750 ml) under N2. To this was added tri-n-butylphosphin (24 ml, 98 mmol) and ADDP (25 g, 98 mmol) resulting in a suspension, which was stirred overnight at 20° C. The mixture was concentrated in vacuo to ˜100 ml, filtered, and the filtrate was evaporated with silica gel. Flash chromatography (EtOAc/heptane 1:4) afforded 24 g of the title compound. LC-MS (m/z): 401 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907096B2
Source datasetuspto-grants-2014_12
ORD IDord-c55cce2106a445f8bc09ca0263e6649b
Source noteuspto-grants-2014_12