HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608711Generated: November 3, 2026
Dimethylformamide → Benzaldehyde, 4-(diphenylamino)-
https://huagongshe.com/reaction/1608711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triphenylamine | HCID 11775 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | 78.4% |
Reaction Steps
Phosphorus oxychloride (MW 153, 0.129M, 19.7 g) was added dropwise to dimethylformamide ("DMF") (MW 73, 0.774M, 56.5 g) maintaining the temperature at <10° C. with external cooling. Triphenylamine (MW 245, 0.129M, 31.5 g) was added and the reaction mixture stirred at 100° C. for 1 hour. After cooling to room temperature and pouring into water (500 ml), the suspension was neutralised to pH 6 with saturated sodium acetate solution. The suspension was filtered off and washed with water, then redissolved in dichloromethane and dried over MgSO4 before screening through Silica gel (MERCK 60H Art 7736) and solvent removed under reduced pressure to give 27.5 g of 4-(N,N-diphenylamino) benzaldehyde (78% yield) as a yellow solid, m.p. 132°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395969 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-a2d3bfb81da4428aa36f23a989458e9e |
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| Source note | uspto-grants-1995_03 |
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