Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787889Generated: October 31, 2026

Triphenylphosphine → Methyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/1787889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantMethyl 4-fluorosalicylateHCID 2775386—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoateHCID 5760250261%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of methyl 4-fluoro-2-hydroxybenzoate (5.1 g, 30 mmol), triphenylphosphine (9.5 g, 36 mmol), 1-tert-butoxycarbonyl-4-hydroxypiperidine (6 g, 30 mmol), and benzene (10 mL) was heated until all solids dissolved. The solution was cooled to 0° C., then sonicated while adding diethyl azodicarboxylate (6.3 g, 36 mmol) dropwise. After the addition was complete, the reaction mixture was sonicated for an additional 60 min, diluted with CH2Cl2 (25 mL), and purified by flash chromatography, eluting with 10% EtOAc in hexanes to yield the title compound (6.45 g, 61%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-5b54b93e44bc459fb114f8396288f7b7
Source noteuspto-grants-2009_03