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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712411Generated: October 31, 2026

alpha-Chloro-m-nitrotoluene → Tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-(3-nitrobenzyloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1712411

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-m-nitrotolueneHCID 12078—
ReactantTert-butyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy) propoxy]phenyl}piperidine-1-carboxylateHCID 15546933—
ProductTert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-(3-nitrobenzyloxy)piperidine-1-carboxylateHCID 68502850—

Reaction Steps

Analogously to Method D, 1.0 g of tert-butyl 3-hydroxy-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate and 0.417 g of 1-chloromethyl-3-nitrobenzene are used to obtain the title compound as a slightly yellowish oil. Rf=0.37 (1:2 EtOAc heptane); Rt=6.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-287a3af4b4ab453d9194d13935223db8
Source noteuspto-grants-2010_09