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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787899Generated: October 29, 2026

Triphenylphosphine → Methyl 2-(1-tert-Butoxycarbonylpiperidin-3-ylmethoxy)-4-isopropylbenzoate

https://huagongshe.com/reaction/1787899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactanttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
ReactantMethyl 4-Isopropyl-2-hydroxybenzoateHCID 59745620—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(1-tert-Butoxycarbonylpiperidin-3-ylmethoxy)-4-isopropylbenzoateHCID 6857335943%

Reaction Steps

The methyl 4-isopropyl-2-hydroxybenzoate (4.4 g, 22.7 mmol) was dissolved in THF (100 mL). Then 3-(hydroxy-methyl)-1-tert-butoxycarbonylpiperidine (4.88 g, 22.7 mmol) and triphenylphosphine (7.14 g, 27.24 mmol) were added. The mixture was placed in an ice bath, and then diisopropyl azodicarboxylate (4.59 g, 22.7 mmol) in methylene chloride (15 mL) was added dropwise. The reaction mixture was allowed to warm gradually to room temperature. After 16 h, the solvent was removed under vacuum. The solid residue was subjected directly to flash chromatography on silica (0 to 30% EtOAc in hexane gradient), giving the title compound (3.34 g, 43% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-f3d29e400cd341f0b5639776912b6bd4
Source noteuspto-grants-2009_03