HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963450Generated: October 30, 2026
2,4-Dichlorobenzylamine → HCID 10617174, compound
https://huagongshe.com/reaction/963450
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichlorobenzylamine | HCID 1485 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 19082438 | HCID 19082438 | — |
| Product | HCID 10617174 | HCID 10617174 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763474 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-3becbea2af56412a9088597a417f52be |
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| Source note | uspto-grants-1998_06 |
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