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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269596Generated: October 24, 2026

Diethyl 2-((tert-butoxycarbonyl)amino)malonate → Diethyl 2-(2-benzyloxy-5-iodobenzyl)-2-tert-butoxycarbonylaminomalonate

https://huagongshe.com/en/reaction/269596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl 2-((tert-butoxycarbonyl)amino)malonateHCID 382219—
ReactantSodium ethoxideHCID 2723922—
Reactant1-Benzyloxy-2-bromomethyl-4-iodobenzeneHCID 11418231—
SolventEthanolHCID 702—
ProductDiethyl 2-(2-benzyloxy-5-iodobenzyl)-2-tert-butoxycarbonylaminomalonateHCID 66879924—

Reaction Steps

41 g (101.7 mmol) of 1-benzyloxy-2-bromomethyl-4-iodobenzene (Example 4A) are added to a solution of 28 g (101.7 mmol) of diethyl 2-[N-(tert-butoxycarbonyl)amino]malonate and 7.9 ml (101.7 mmol) of sodium ethoxide in 300 ml of ethanol. After stirring at RT for 3 h, the precipitated product is collected by suction filtration. After drying in vacuo, 55 g (90% of theory) of product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446102B2
Source datasetuspto-grants-2008_11
ORD IDord-8c030366cae84f828a34666b360855c4
Source noteuspto-grants-2008_11