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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482227Generated: October 26, 2026

1-Bromo-3-chloropropane → 10-(3-Chloropropyl)-10H-phenoxazine

https://huagongshe.com/reaction/482227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantPhenoxazineHCID 67278—
SolventDimethylformamideHCID 6228—
Product10-(3-Chloropropyl)-10H-phenoxazineHCID 10083926—

Reaction Steps

To a solution of phenoxazine (3.7 g, 0.02 mol) in dry dimethylformamide (100 ml) kept under an atmosphere of nitrogen, sodium hydride (1.2 g, 0.03 mol, 60% dispersion in oil) was carefully added. The reaction mixture was left stirring for 15 minutes. 1-Bromo-3-chloro-propane (8.0 g, 0.05 mol) was added and the mixture was left stirring overnight. Ammonium chloride (2.0 g, 0.04 mol) was added, and after continued stirring for 30 minutes, the solution was poured onto water (300 ml). The mixture was extracted with dichloromethane (2×200 ml). The combined organic extracts were dried (MgSO4), filtered and the solvent evaporated in vacuo. 10-(3-Chloropropyl)-10H-phenoxazine was obtained in quantitative yield as an oil and used without further purification. Rf : 0.68 (SiO2 ; n-heptane/ethyl acetate=1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05795888
Source datasetuspto-grants-1998_08
ORD IDord-7ed09a21816e4c048b99ebc8a7cc8cb7
Source noteuspto-grants-1998_08