HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039838Generated: October 26, 2026
Hydrochloric Acid → 4-Dibenzylamino-2,5-dimethylbenzaldehyde
https://huagongshe.com/reaction/1039838
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dibenzyl-(4-iodo-2,5-dimethylphenyl)amine | HCID 57461072 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Dibenzylamino-2,5-dimethylbenzaldehyde | HCID 57461074 | 49.9% |
Reaction Steps
To a stirred solution of dibenzyl-(4-iodo-2,5-dimethylphenyl)amine (9.35 g, 21.9 mmol) in toluene (100 mL) under nitrogen at −15° C. was added n-butyllithium in hexanes (1.6 M, 20.5 mL, 32.8 mmol) dropwise via syringe over a 30 min period. The resulting mixture was stirred at −15° C. for 15 min and then N,N-dimethylformamide (1.86 mL, 24.1 mmol) was added dropwise over a 10 min period. After 2 h, aqueous hydrochloric acid (1 M, 46.6 mL) and brine (30 mL) were added and the resulting mixture was stirred for 15 min. The layers were separated and the organic layer was extracted with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-50% DCM in hexanes) to give the title compound (3.60 g, 49% yield) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551978B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-953435f1ed2a436f9f07fae3eee38af6 |
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| Source note | uspto-grants-2013_10 |
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