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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712522Generated: November 2, 2026

1-(3-Bromopropoxy)-3-fluorobenzene → tert-Butyl 3-{2-[2-(2-acetylaminoethyl)-5-fluorophenoxy]ethoxy}-4-{4-[3-(3-fluorophenoxy)propoxy]phenyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1712522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromopropoxy)-3-fluorobenzeneHCID 23294433—
ReactantHCID 68504580HCID 68504580—
Producttert-Butyl 3-{2-[2-(2-acetylaminoethyl)-5-fluorophenoxy]ethoxy}-4-{4-[3-(3-fluorophenoxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68505109—

Reaction Steps

Analogously to Method I, 0.26 g of tert-butyl 3-{2-[2-(2-acetylaminoethyl)-5-fluorophenoxy]ethoxy}-4-(4-hydroxyphenyl)piperidine-1-carboxylate and 0.153 g of 1-(3-bromopropoxy)-3-fluorobenzene are reacted. The title compound is obtained as a yellowish oil. Rf=0.41 (EtOAc); Rt=5.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-d0391636d22e4cc39a2e73b706f0f4f2
Source noteuspto-grants-2010_09