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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963450Generated: October 30, 2026

2,4-Dichlorobenzylamine → HCID 10617174, compound

https://huagongshe.com/reaction/963450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzylamineHCID 1485—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 19082438HCID 19082438—
ProductHCID 10617174HCID 1061717440%

Reaction Steps

A solution of 3-butoxy-4-(1,1-dimethyl-propylamino)-cyclobut-3-ene-1,2-dione (7.18 g, 30 mmol, Example 5) and 2,4-dichlorobenzylamine (5.28 g, 30 mmol) in tetrahydrofuran (40 mL) was stirred at room temperature for 16 hours. The solvent was removed and the residue was triturated thoroughly with diethyl ether and dried to give 8.94 g of a crude product. Successive recrystallizations of this material from acetonitrile (charcoal), acetonitrile (twice), acetone (charcoal) and acetone (twice) afforded 4.08 g (40%) of the title compound as a white, electrostatic solid: mp 196°-197° C. (softens 188° C.); 1H NMR (DMSO-d6): δ 7.81 (m, 1H), 7.68 (m, 1H), 7.48 (m, 3H), 4.81 (d, 2H), 1.67 (m, 2H), 1.31 (s, 6H), 0.82 (t, 3H) ppm. IR (KBr): 3210, 1790, 1645 cm-1 ; MS (m/z) 340/342/344 (M+). HPLC indicates a major component (99% ). Differential scanning calorimetry studies indicate that this material is a mixture of crystal forms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763474
Source datasetuspto-grants-1998_06
ORD IDord-3becbea2af56412a9088597a417f52be
Source noteuspto-grants-1998_06