HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819919Generated: October 26, 2026
Pyridine → 1-Tert-butyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea
https://huagongshe.com/reaction/1819919
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butyl isocyanate | HCID 62412 | — |
| Reactant | 6,7,8,9-Tetrahydro-dibenzofuran-2-ylamine | HCID 2794782 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Tert-butyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea | HCID 24897858 | 49.6% |
Reaction Steps
tert-Butylisocyanate (0.55 g, 5.5 mmol) was added to a cooled (0° C.) solution of 6,7,8,9-tetrahydro-dibenzofuran-2-ylamine (0.94 g, 5.0 mmol) in tetrahydrofuran (20 mL). The reaction mixture was stirred for 10 minutes at 0° C. and then allowed to warm to ambient temperature for 5 hours. An additional portion of tert-butylisocyanate (0.65 mL) was added the reaction mixture was stirred overnight. The reaction was incomplete, so pyridine (10 mL) was added and the reaction mixture was heated to reflux for 4.5 hours and then concentrated under reduced pressure. The crude material was dissolved in ethyl acetate and washed with 1 N HCl, water, and brine, dried (Na2SO4) and concentrated. The crude material was recrystallized from acetonitrile to provide 1-tert-butyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea (0.71 g). Mp 310-312° C. (DEC); Anal. Calcd. for C17H22N2O2: C, 71.30; H, 7.74; N, 9.78; Found: C, 71.18; H, 7.84; N, 9.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601856B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-06ff6d1d31a64478836532d68357153d |
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| Source note | uspto-grants-2009_10 |
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