HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675250Generated: November 2, 2026
Dimethylformamide → 2-Bromo-4-(bromomethyl)-1-(trifluoromethoxy)benzene
https://huagongshe.com/reaction/1675250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | 3-Bromo-4-(trifluoromethoxy)benzyl alcohol | HCID 26597851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-4-(bromomethyl)-1-(trifluoromethoxy)benzene | HCID 59300671 | 99.4% |
Reaction Steps
To a solution of (3-bromo-4-(trifluoromethoxy)phenyl)methanol 19.1 (6.78 g, 25 mmol) in 30 mL of DCM, was added DMF (0.5 mL) and thionyl bromide (2 mL, 26 mmol). The mixture was stirred at 23° C. for 4 hours. DCM (120 mL) was added to the reaction mixture, and the resulting mixture was washed with aqueous saturated NaHCO3. The organic layer was dried over Na2SO4 and concentrated to give 19.2 (8.3 g, 99% yield) as a yellow oil, which was used directly in the next step without further purification. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.74 (1 H, d, J=2.0 Hz), 7.38-7.53 (2 H, m), 4.53 (2 H, d, J=5.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003648B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-fb35d70ac3884ffeaeef6ab62794a941 |
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| Source note | uspto-grants-2011_08 |
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