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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445439Generated: October 30, 2026

Triphenylphosphine → methyl 4-(tert-butyl)-2-(1-Boc-piperidin-4-yloxy)benzoate

https://huagongshe.com/reaction/1445439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantMethyl 4-tert-butyl-2-hydroxybenzoateHCID 20777194—
SolventTetrahydrofuranHCID 8028—
Productmethyl 4-(tert-butyl)-2-(1-Boc-piperidin-4-yloxy)benzoateHCID 68532357—

Reaction Steps

To a stirring solution of methyl 4-tert-butyl-2-hydroxybenzoate (9.45 g, 45.4 mmol), 1-Boc-piperidin-4-ol (9.6 g, 47.7 mmol) and triphenylphosphine (12.5 g, 47.7 mmol) in THF (125 mL) was added, dropwise via an addition funnel, a solution of diisopropyl azodicarboxylate (9.4 mL, 47.7 mmol) in THF (25 mL). After 72 h, the solvent was removed in vacuo and the residue was dissolved in a minimal amount of chloroform and vacuum filtered through a pad of silica gel, eluting with a solution of 20% ethyl acetate in hexanes. The filtrate was then concentrated in vacuo and the residue was chromatographed over silica gel, eluting with a gradient of 5% ethyl acetate in hexanes through 20% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo to give the ether (12.9 g, 73%) as a thick colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666866B2
Source datasetuspto-grants-2010_02
ORD IDord-da54c21c25e54c848c908cd24b37f284
Source noteuspto-grants-2010_02