Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374603Generated: November 2, 2026

1-Bromo-3-chloropropane → HCID 58737337, compound

https://huagongshe.com/reaction/2374603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58737289HCID 58737289—
SolventWaterHCID 962—
ProductHCID 58737337HCID 58737337—

Reaction Conditions

Temperature60 °C

Reaction Steps

60% Oily sodium hydride (832 mg) was added to a solution of ethyl (±)-1,3-dimethyl-2,5-dioxo-2,3,5,6,7,8-hexahydro-1H-naphtho[2,3-d]imidazole-6-carboxylate (5.0 g) obtained in Reference Example 138 in dimethylformamide,and the mixture was stirred at 60° C. for 1 hour. 1-Bromo-3-chloropropane was added thereto, and the mixture was stirred at 60° C. for 4 hours. The reaction mixture was allowed to cool, and water was added to decompose excessive sodium hydride. Then, the mixture was extracted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462628B2
Source datasetuspto-grants-2008_12
ORD IDord-2b128f4241cd4414a7bc46757f5ee8a4
Source noteuspto-grants-2008_12