Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963448Generated: October 27, 2026

2,4-Dichlorobenzylamine → 3-(2,4-Dichlorobenzylamino)-4-(1,2,2-trimethylproylamino)-cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/963448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzylamineHCID 1485—
Reactant3-Butoxy-4-(1,2,2-trimethyl-propylamino)-cyclobut-3-ene-1,2-dioneHCID 54135011—
SolventTetrahydrofuranHCID 8028—
Product3-(2,4-Dichlorobenzylamino)-4-(1,2,2-trimethylproylamino)-cyclobut-3-ene-1,2-dioneHCID 1908243929%

Reaction Steps

Tetrahydrofuran (10 mL), 3-butoxy-4-(1,2,2-trimethyl-propylamino)-cyclobut-3-ene-1,2-dione (1.01 g, 3.99 mmol, Example 1) and 2,4-dichlorobenzylamine (0.70 g, 4.0 mmol) were stirred together at room temperature for 14 hours. Following removal of solvent, the residue was triturated with diethyl ether and dried. The off-white solid product was recrystallized twice from nitromethane to yield 0.408 g (29%) of the title compound as a white solid: mp 234°-235° C.; 1H NMR: (DMSO-d6): δ 7.67 (m, br, 1H), 7.65 (m, br, 1H), 7.48 (m, 2H), 7.32 (m, br, 1H), 4.80 (m, 2H), 3.90 (m, 1H), 1.10 (d, 3H), 0.86 (s, 9H) ppm. IR (KBr): 3140, 1790, 1640 cm-1 ; MS (m/z): 354/356/358. HPLC indicates a major component (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763474
Source datasetuspto-grants-1998_06
ORD IDord-38a901a6f98d49ccb8c1551a3223aea0
Source noteuspto-grants-1998_06