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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061086Generated: November 2, 2026

Ammonium Chloride → 1-vinyl-13-oxabicyclo[10.1.0]tridecane

https://huagongshe.com/reaction/1061086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Reactant2-ChlorocyclododecanoneHCID 566533—
ReactantHCID 178461836HCID 178461836—
SolventTetrahydrofuranHCID 8028—
Product1-vinyl-13-oxabicyclo[10.1.0]tridecaneHCID 507393882.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A four-neck flask equipped with a thermometer, stirrer and condenser tube was charged with 100 g (0.46 mol) of 2-chlorocyclododecanone and 122 g of tetrahydrofuran, and at −10 to 0° C., a THF solution of vinylmagnesium chloride (0.82 mol) was added dropwise. The mixture was allowed to stand for reaction for 30 minutes, and 420 g (3.27 mol) of N,N′-dimethylpropyleneurea (DMPU) was added. The mixture was heated to 50° C. and allowed to stand for reaction for 1 hour, and saturated ammonium chloride aqueous solution was added dropwise for inactivation. The reaction mixture was subjected to extraction with hexane, and the solvent was recovered. The residue was distilled to obtain 1-vinyl-13-oxabicyclo[10.1.0]tridecane (80 g, 0.38 mol, chemical purity 98%, cis form:trans form=88:12). The yield was 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525207B1
Source datasetuspto-grants-2003_02
ORD IDord-7a9a8a67641344f88f5dca5e0e08be22
Source noteuspto-grants-2003_02