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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-Butyl isocyanateHCID 62412—
Reactant6,7,8,9-Tetrahydro-dibenzofuran-2-ylamineHCID 2794782—
SolventTetrahydrofuranHCID 8028—
Product1-Tert-butyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-ureaHCID 2489785849.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601856B2
Source datasetuspto-grants-2009_10
ORD IDord-06ff6d1d31a64478836532d68357153d
Source noteuspto-grants-2009_10