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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772460Generated: October 26, 2026

4-Bromobenzamide → HCID 178484323, compound

https://huagongshe.com/reaction/1772460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzamideHCID 69683—
ReactantDimethylformamide dimethyl acetalHCID 78373—
SolventDiethyl EtherHCID 3283—
ProductHCID 178484323HCID 17848432371.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Bromo benzamide (28.0 g, 0.140 mol) was suspended in 1,1-dimethoxy-N,N-dimethylmethanamine (50 mL, 420 mmol) and the solution was stirred and heated to 90° C. for 2 hours. The solution was then cooled to ambient temperature and diethyl ether (150 mL) was added. The solution was cooled to 0° C. overnight and filtered to give (E)-4-bromo-N-((dimethylamino)methylene)benzamide as a colorless solid (25.6 g). This material was then dissolved in acetic acid (50 mL) and hydrazine (3.50 g, 110 mmol) was added slowly (exotherm) to the stirred solution, which solidified. The mixture was heated to 90° C. and a stir bar was added. The solid slowly dissolved over 8 hours and was then cooled to ambient temperature and the solution was diluted with water (35 mL). The resulting white solid was filtered and dried in vacuo to furnish the title compound as a colorless solid (19.8 g, 88%): 1H NMR (400 MHz, DMSO-d6) δ 13.91 (s, 1H), 8.51 (s, 1H), 8.01-7.93 (m, 2H), 7.73-7.67 (m, 2H; ESIMS m/z 224, 226 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249133B2
Source datasetuspto-grants-2016_02
ORD IDord-18195c0c5ee04bf4b2adb14d926e33cf
Source noteuspto-grants-2016_02