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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176336Generated: November 1, 2026

1-Chloro-4-methoxybutane → tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{[(4-methoxybutyl)phenyl-carbamoyl]methoxy}piperidine-1-carboxylate

https://huagongshe.com/reaction/1176336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-methoxybutaneHCID 87363—
ReactantHCID 68502337HCID 68502337—
Producttert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{[(4-methoxybutyl)phenyl-carbamoyl]methoxy}piperidine-1-carboxylateHCID 68502357—

Reaction Steps

Analogously to Example 2c, 0.49 g of tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-phenylcarbamoylmethoxypiperidine-1-carboxylate (Example 62b) and 0.37 g of 1-chloro-4-methoxybutane are reacted. The title compound is obtained as a yellow oil. Rf=0.20 (1:1 EtOAc-heptane); Rt=5.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-b07c9aaaed3c464897cfdbc99eb52409
Source noteuspto-grants-2010_11