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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 5-Bromosalicylic acid | HCID 6972 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HOAt | HCID 181649 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-N,N-diethyl-2-hydroxybenzamide | HCID 24285295 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426447B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-b18d29ca88ca4e7a9a4d179899743626 |
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| Source note | uspto-grants-2013_04 |
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