HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609576Generated: October 31, 2026
N,N-Dimethylaniline → HCID 53939820, compound
https://huagongshe.com/reaction/1609576
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | Octodrine | HCID 10982 | — |
| Reactant | 2-Dibenzofuranol | HCID 66587 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 53939820 | HCID 53939820 | 130.3% |
Reaction Steps
A solution of 2-hydroxydibenzofuran (5.0 g, 27 mmol) and dimethylaniline (3.4 mL, 27 mmol) in 35 mL of benzene plus 1.5 mL of dioxane was added dropwise under nitrogen to a solution of trichloromethyl chloroformate (1.6 mL, 14 mmol) in 30 mL of benzene at ice bath temperature. After the addition the cooling bath was removed and the stirring continued for approximately 24 hours. The reaction was cooled to ice bath temperature and a solution of 1,5-dimethylhexylamine (4.6 mL, 27 mmol) and pyridine (4.4 mL, 54 mmol) in 30 mL of benzene was added dropwise over 15 minutes. After the addition the reaction was stirred at ice bath temperature for 2 hours. The cooling bath was removed and the stirring continued for approximately 22 hours. The reaction was extracted two times with 1N HCl. The organic solution was dried over anhydrous MgSO4 and the solvent removed under reduced pressure to give 6.19 g of a yellow solid. Recrystallization from isopropanol gave 4.27 g (46%) of the title compound as a yellow crystalline solid, mp 114°-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401769 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-606c7fde20c64b2d969872aa39a406a9 |
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| Source note | uspto-grants-1995_03 |
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