HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177148Generated: October 30, 2026
Carbon Tetrachloride → HCID 90417935, compound
https://huagongshe.com/reaction/2177148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Methoxy-2-methyl-3-(trifluoromethyl)benzene | HCID 46737517 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 90417935 | HCID 90417935 | — |
Reaction Steps
Into a 50-mL round-bottom flask, was placed 1-methoxy-2-methyl-3-(trifluoromethyl)benzene (700 mg, 3.68 mmol, 1.00 equiv), CCl4 (3.0 mL). The mixture was cooled to 0° C. Br2 (698 mg, 4.37 mmol, 1.19 equiv) and AcOH (0.5 mL) were added. The resulting solution was stirred for 1 h at 30° C. The reaction process was monitored by TLC (Petroleum ether). The reaction was then quenched by the addition of 10 mL of saturated sodium bicarbonate. The resulting solution was extracted with 3×10 mL of dichloromethane and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with petroleum ether. This resulted in 0.7 g (71%) of 1-bromo-4-methoxy-3-methyl-2-(trifluoromethyl)benzene as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067898B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-7419e5834fa94803ad3558f176e5cc41 |
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| Source note | uspto-grants-2015_06 |
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