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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612830Generated: November 3, 2026

Bromodiphenylmethane → 4-Diphenylmethoxy-1-[4-(2-nitrophenoxy)butyl]piperidine

https://huagongshe.com/reaction/1612830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromodiphenylmethaneHCID 236603—
Reactant4-Hydroxy-1-[4-(2-nitrophenoxy)butyl]piperidineHCID 19776729—
Reactant4-Hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidineHCID 19776793—
Product4-Diphenylmethoxy-1-[4-(2-nitrophenoxy)butyl]piperidineHCID 19776833—

Reaction Steps

The procedure of Example 1 (a) was repeated except for using diphenylmethylbromide and 4-hydroxy-1-[4-(2-nitrophenoxy)butyl]piperidine instead of diphenylmethyl bromide and 4-hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine to give oily 4-diphenylmethoxy-1-[4-(2-nitrophenoxy)butyl]piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190959
Source datasetuspto-grants-1993_03
ORD IDord-486c4bc3f05a42df88ddb744972c0c92
Source noteuspto-grants-1993_03