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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377784Generated: October 30, 2026

Ethyl orthoformate → 1-benzyl-4,5-dihydro-1H-imidazole

https://huagongshe.com/reaction/2377784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantN-BenzylethylenediamineHCID 77801—
ReactantHCID 69224605HCID 69224605—
Product1-benzyl-4,5-dihydro-1H-imidazoleHCID 10877422—

Reaction Steps

As shown in FIG. 9B (Scheme 4), the synthesis of 1-(3-aminopropyl)-3-benzylimidazolidin-2-one (35) will be performed by treating the starting material N1-benzylethane-1,2-diamine with diethoxymethoxyethane to form 1-benzyl-4,5-dihydro-1H-imidazole. The imidazole intermediate will be treated with BuLi (forming a lithiate) followed by quenching with water to form the final intermediate 1-benzylimidazolidin-2-one. Treating the imidazolidinone with NaH followed by Br—(CH2)3—N(SiMe3)2 under reducing conditions will afford the intermediate 35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470703B1
Source datasetuspto-grants-2008_12
ORD IDord-79d5c8a412904410b706e10077374923
Source noteuspto-grants-2008_12