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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088475Generated: November 2, 2026

1-Bromo-3-chloropropane → HCID 67777211, compound

https://huagongshe.com/reaction/2088475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
Reactantpyrrolo[1,2-a]quinoxalin-4(5H)-oneHCID 2740936—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67777211HCID 67777211—
ProductPyrrolo[1,2-a]quinoxalin-4(5H)-one, 5-(3-chloropropyl)-HCID 67777358—

Reaction Conditions

Temperature80 °C

Reaction Steps

Pyrrolo[1,2-a]quinoxalin-4(5H)-one (500 mg; 2.71 mmol) was dissolved in anhydrous DMF (10 mL) in a 25 mL round bottomed flask. NaH (68.6 mg; 2.71 mmol; 95%) was carefully added to the flask under a blanket of nitrogen. The reaction mixture was allowed to react for 2 h at room temperature after which 1-bromo-3-chloropropane (511.99 mg, 3.25 mg) was added and the mixture was heated to 80° C. overnight. The reaction mixture was diluted with ethyl acetate and washed with H2O, brine, dried over sodium sulfate, then filtered and concentrated. The crude mixture was purified by flash chromatography to yield the desired 5-(3-chloropropyl)pyrrolo[1,2-a]quinoxalin-4(5H)-one and 5-(3-bromopropyl)pyrrolo[1,2-a]quinoxalin-4(5H)-one in approximately a 60:40 ratio. The mixture was used in the next step without further purification. [M+1]+=261 Chloride; [M+1]+=305 Bromide. 1H NMR (CDCl3): δ 2.18-2.42 (2H); 3.49-3.62 (1H); 3.63-3.81 (1H); 4.38-4.50 (2H); 6.61-6.71 (1H); 7.13-7.514 (4H); 7.65-7.80 (2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435993B2
Source datasetuspto-grants-2013_05
ORD IDord-d94a59bbef75441c9cfe19ad23229740
Source noteuspto-grants-2013_05