HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730382Generated: October 25, 2026
4-Bromophenacyl bromide → HCID 178441576, compound
https://huagongshe.com/reaction/730382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propanimidamide, 2,2-dimethyl-, hydrochloride (1:1) | HCID 2781880 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178441576 | HCID 178441576 | 81% |
Reaction Steps
A solution of 2,4′-dibromoacetophenone (4.17 g, 15.0 mmol) in N,N-dimethylformamide (60.0 mL) was treated with t-butylcarbamidine hydrochloride (2.05 g, 15.0 mmol) and K2CO3 (4.15 g, 30.0 mmol) and heated to 50° C. for 4 h. Following cooling, the reaction was quenched with water, diluted with brine, and extracted thrice with EtOAc. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. Purification via flash column chromatography (10-40% EtOAc/hexanes) gave the title compound as a light yellow solid (3.38 g; 81%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.58 (d, J=8.1 Hz, 2 H) 7.46 (d, J=8.6 Hz, 2 H) 7.18 (s, 1 H) 1.42 (s, 9 H). MS(ES+) m/e 279/281 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582668B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-c87a607869694ce893c90854d6234359 |
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| Source note | uspto-grants-2009_09 |
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