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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176556Generated: October 30, 2026

4-Hydroxyisobenzofuran-1(3H)-one → tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(1-oxo-1,3-dihydroisobenzofuran-4-yloxy)ethoxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1176556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxyisobenzofuran-1(3H)-oneHCID 12662077—
ReactantTert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylateHCID 86609984—
Producttert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(1-oxo-1,3-dihydroisobenzofuran-4-yloxy)ethoxy]piperidine-1-carboxylateHCID 68570413—

Reaction Steps

Analogously to Method G, 0.210 g of tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylate (Example 14b) and 0.094 g of 4-hydroxy-3H-isobenzofuran-1-one are reacted. The title compound is obtained as a white solid. Rf=0.32 (1:1 EtOAc-heptane); Rt=5.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-cbb7ff99df114ec88865c23edce09f0f
Source noteuspto-grants-2010_11