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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819920Generated: October 26, 2026

Diethylcarbamoyl chloride → 1,1-Diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea

https://huagongshe.com/reaction/1819920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
Reactant6,7,8,9-Tetrahydro-dibenzofuran-2-ylamineHCID 2794782—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
Product1,1-Diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-ureaHCID 2489807554.5%

Reaction Steps

Diethylcarbamoyl chloride (0.72 mL, 5.5 mmol) was added to a solution of 6,7,8,9-tetrahydro-dibenzofuran-2-ylamine (0.94 g, 5.0 mmol) in pyridine (15 mL). The reaction mixture was stirred overnight at room temperature. The crude material was diluted in chloroform and washed with 1 N HCl, water, and brine, dried (Na2SO4) and concentrated. The crude material was recrystallized from acetonitrile to provide 1,1-diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea (0.78 g). Mp 179-180° C.; Anal. Calcd. for C17H22N2O2: C, 71.30; H, 7.74; N, 9.78; Found: C, 71.29; H, 7.66; N, 9.72.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601856B2
Source datasetuspto-grants-2009_10
ORD IDord-b5f848d6e7b44f8ba556ec37dba7bf2f
Source noteuspto-grants-2009_10