HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058645Generated: October 31, 2026
Water → 4-(N,N-diphenylaminomethyl)benzaldehyde
https://huagongshe.com/reaction/1058645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-(4-bromobenzyl)diphenylamine | HCID 18669015 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(N,N-diphenylaminomethyl)benzaldehyde | HCID 86758833 | 57% |
Reaction Steps
In an argon atmosphere, the thus obtained N-(4-bromobenzyl)diphenylamine (440 mg, 1.30 mmol) was dissolved in tetrahydrofuran (6 mL) and cooled to −78° C. A 1.6 M n-butyl lithium hexane solution (1.3 mL, 2.0 mmol) was added thereto, and, 5 minutes thereafter, dimethylformamide (0.20 mL, 2.6 mmol) was further added thereto, followed by stirring for 5 minutes. To the reaction solution was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (9:1 hexane/ethyl acetate) to obtain 4-(N,N-diphenylaminomethyl)benzaldehyde (213 mg, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518268B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-6934cce5d46f4c62a944070c294d87b8 |
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| Source note | uspto-grants-2003_02 |
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