HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612652Generated: October 30, 2026
N,N-Dimethylaniline → HCID 19776529, compound
https://huagongshe.com/reaction/1612652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19776529 | HCID 19776529 | 124.4% |
Reaction Steps
Trichloromethyl chloroformate (3.54 mL, 29.4 mmol) is added dropwise under a nitrogen atmosphere to a solution of 2-phenylphenol (10.0 g, 58.8 mmol) in 150 mL of benzene at room temperature. After the addition, dimethylaniline (7.45 mL, 58.8 mmol) is added dropwise at such a rate that the temperature of the reaction mixture is maintained between 20°-25° C. The resulting mixture is stirred at room temperature for 3 hours. A solution of 4-methylpiperidine (6.95 mL, 58.8 mmol) and dimethylaniline (7.45 mL, 58.8 mmol) in 50 mL of benzene is then added dropwise. After the addition the reaction is stirred at room temperature overnight. The reaction mixture is washed with 1N HCl, 5% NaHCO3, dried (MgSO4) and the solvent removed under reduced pressure. Purification of the crude reaction product by HPLC (hexane-methylene chloride) followed by recrystallization from diisopropyl ether gives the title compound as a white crystalline solid (10.8 g, 62), mp 85° -86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05190940 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-3f4ff06bdac047e788493c851a10eb06 |
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| Source note | uspto-grants-1993_03 |
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