HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866078Generated: October 31, 2026
1-Bromo-4-(trifluoromethoxy)benzene → HCID 19040924, compound
https://huagongshe.com/reaction/866078
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-(trifluoromethoxy)benzene | HCID 521008 | — |
| Reactant | HCID 764508 | HCID 764508 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19040924 | HCID 19040924 | 4.7% |
Reaction Steps
This compound was prepared in a manner analogous to that of Step B of Example 3, with 2.0 grams (0.008 mole) of ethyl N-(thien-2-ylmethyl)piperidin-4-ylcarboxylate, 3.5 mL (0.024 mole) of 4-trifluoromethoxyphenyl bromide, and 0.6 gram (0.025 gram-atom) of magnesium turnings in about 69 mL of tetrahydrofuran as reagents. The crude reaction product was subjected to column chromatography on silica gel, with pure methylene chloride, 9:1 methylene chloride:acetone, pure acetone, and then 8:2 methylene chloride:acetone as eluants. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 0.2 gram of N-(thien-2-ylmethyl)-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05569664 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-0b4dfeb2292242cbbc852add7b738d1a |
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| Source note | uspto-grants-1996_10 |
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