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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383264Generated: October 30, 2026

1,2-Dibromoethane → 5-Bromo-2-(2-bromoethoxy)aniline

https://huagongshe.com/reaction/383264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-4-BromophenolHCID 351840—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(2-bromoethoxy)anilineHCID 6697764437%

Reaction Steps

A mixture of the product 2-amino-4-bromophenol (500 mg, 2.66 mmol), 1,2-dibromoethane (2.5 g, 13.3 mmol) and K2CO3 (1.84 g, 13.3 mmol) in DMF (10 mL) was stirred at room temperature for 4 h. The mixture was diluted with water (100 mL) and extracted with ethyl acetate (100 mL). The organic layer was washed with water (3×50 mL) and brine (50 mL), concentrated and purified by column chromatography on silica gel (ethyl acetate in petroleum, 10% v/v) to give 5-bromo-2-(2-bromoethoxy)benzenamine (250 mg, 37%) as a yellow solid. LCMS: 294 [M+1]+. 1H NMR (400 MHz, DMSO-d6) δ 3.79 (t, J=6.0 Hz, 2H), 4.25 (t, J=5.6 Hz, 2H), 5.06 (s, 2H), 6.63 (dd, J1=2.4 Hz, J2=8.0 Hz, 1H), 6.77 (d, J=8.4 Hz, 1H), 6.82 (d, J=2.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367663B2
Source datasetuspto-grants-2013_02
ORD IDord-d4d6425292714c3baff81e2eaa12c49e
Source noteuspto-grants-2013_02