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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899057Generated: November 1, 2026

5-(N,N-bis(2-chloroethyl)amino)-2,4-dinitrobenzamide → 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzonitrile

https://huagongshe.com/reaction/1899057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(N,N-bis(2-chloroethyl)amino)-2,4-dinitrobenzamideHCID 126690—
SolventNitrogenHCID 947—
SolventThionyl ChlorideHCID 24386—
Product5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzonitrileHCID 37256687%

Reaction Steps

A solution of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (1) (VII) (0.20 g, 0.57 mol) in SOCl2 (5 mL) was heated under reflux in N2 for 84 h. Excess SOCl2 was removed under reduced pressure, and the residue was chromatographed on silica gel. Elution with EtOAc/petroleum ether (3:7) gave 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzonitrile (7) (Ic: X=Cl, R=CN) (0.16 g, 87%), mp (CHCl3) 127° C. 1H NMR (CD3COCD3) δ 8.79 (s, 1 H, H-3), 8.19 (s, 1 H, H-6), 3.93 (s, 8 H, NCH2CH2Cl). 13C NMR δ 148.55 (C-5), 140.98, 139.07 (C-2,4), 129.50, 126.10 (C-3,6), 115.05 (C-1), 112.84 (CN), 54.18 (CH2N), 42.20 (CH2Cl). Anal. (C11H10Cl2N4O4) C,H,N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571845
Source datasetuspto-grants-1996_11
ORD IDord-3814befa580844bcafae13b0fa2e7feb
Source noteuspto-grants-1996_11