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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970262Generated: November 2, 2026

1,2-Dichloroethane → 5-bromo-N,N-diethyl-2-hydroxybenzamide

https://huagongshe.com/reaction/1970262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant5-Bromosalicylic acidHCID 6972—
ReactantDiethylamineHCID 8021—
ReactantHOAtHCID 181649—
SolventDimethylformamideHCID 6228—
Product5-bromo-N,N-diethyl-2-hydroxybenzamideHCID 24285295—

Reaction Conditions

Temperature50 °C

Reaction Steps

Diethylamine (2.39 mL, 23.0 mmol) was added to a solution of 5-bromosalicylic acid (1.000 g, 4.61 mmol), EDC (1.33 g, 6.91 mmol), HOAt (0.627 g, 4.61 mmol) and DMF (20.0 mL) and the system was flushed with argon. The tube was sealed and the mixture stirred at 50° C. for 12 h. The reaction mixture was partitioned between ethyl acetate and water. The aqueous phase was separated and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford a brown oil. This oil was purified via column chromatography on silica gel (RediSep 40 g column, gradient elution with 0-50% ethyl acetate-hexane) to afford 5-bromo-N,N-diethyl-2-hydroxybenzamide as an off-white solid. MS m/z=272.1, 274.1 [M+H]+. Calcd for C11H14BrNO2: 272.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426447B2
Source datasetuspto-grants-2013_04
ORD IDord-b18d29ca88ca4e7a9a4d179899743626
Source noteuspto-grants-2013_04