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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243356Generated: October 30, 2026

Tert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate → 4-(Aminomethyl)benzonitrile hydrochloride

https://huagongshe.com/reaction/1243356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamateHCID 3683768—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Product4-(Aminomethyl)benzonitrile hydrochlorideHCID 9942250—

Reaction Steps

4-cyanobenzylamine hydrochloride (EX-59A) was prepared from 10 g (0.030 moles) of 4-{N,N-bis-(tert-butoxycarbonyl)aminomethyl}benzonitrile, prepared following Synthetic Communication, 28(23), 4419–4429 (1998), by stirring it in 4N HCl Dioxane (75 ml). After 3 h, the solution was concentrated in vacuo and triturated with ether. The solid was collected by filtration and vacuum dried to yield 5 g (98%) of EX-59A as a white solid: 1H NMR (DMSO) d 8.68 (br s, 2H), 7.84 (m, 2H), 7.67 (m, 2H), 4.06 (s, 2H); HRMS (EI) calcd for C8H8N2 133.0766, found 133.0807

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119094B1
Source datasetuspto-grants-2006_10
ORD IDord-be95f0885f73452bae4d6d1b75957a49
Source noteuspto-grants-2006_10