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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655563Generated: October 31, 2026

tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate → 4'-(Aminomethyl)-biphenyl-2-carboxylic acid 1,1-dimethylethyl ester

https://huagongshe.com/reaction/1655563

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylateHCID 9906257—
ReactantHCID 178418441HCID 178418441—
CatalystPalladiumHCID 23938—
Product4'-(Aminomethyl)-biphenyl-2-carboxylic acid 1,1-dimethylethyl esterHCID 9971073—
ProductHCID 19792037HCID 19792037—

Reaction Steps

Following the procedures described in Example 1A, replacing N-triphenylmethyl-5-[2-(4'-bromomethyl)biphenyl)]tetrazole with t-butyl 4'-bromomethyl-biphenyl-2-carboxylate, prepared as described by D. J. Carini, et al. in European Patent Application Number 324,377, published Jul. 19, 1989, the intermediate t-butyl 4'-azidomethyl-biphenyl-2-carboxylate is prepared. The intermediate azidomethyl compound is then hydrogenated as described in Example 1B, using palladium on carbon catalyst instead of Lindlar catalyst, to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250548
Source datasetuspto-grants-1993_10
ORD IDord-674be420fae14e75862503b732b4b9eb
Source noteuspto-grants-1993_10