Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926697Generated: October 30, 2026

Diethyl acetamido(4-bromo-2-nitrobenzyl)malonate → HCID 59627195, compound

https://huagongshe.com/reaction/1926697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl acetamido(4-bromo-2-nitrobenzyl)malonateHCID 10622552—
ReactantHCID 59627070HCID 59627070—
ReactantHCID 59627186HCID 59627186—
ProductHCID 59627195HCID 59627195—

Reaction Steps

Diethyl acetamido(5-chloro-3-methyl-2-nitrobenzyl)malonate (39) Following the procedure for the preparation of diethyl acetamido(4-bromo-2-nitrobenzyl)malonate (24) in Example 5,1-(bromomethyl)-5-chloro-3-methyl-2-nitrobenzene (38) was converted to the title product, which was obtained as a solid (65%). LCMS m/z 401.0 (M+1). 1H NMR (400 MHz, DMSO-d6) δ 1.15 (t, J=7.1 Hz, 6H), 1.90 (s, 3H), 2.24 (br s, 3H), 3.53 (s, 2H), 4.10-4.17 (m, 4H), 7.05 (br d, J=2.2 Hz, 1H), 7.56 (apparent dd, J=2.3, 0.7 Hz, 1H), 8.31 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183238B2
Source datasetuspto-grants-2012_05
ORD IDord-a00c580d85434550b904cfe1d30e688f
Source noteuspto-grants-2012_05