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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
ReactantHCID 764508HCID 764508—
ReactantMagnesiumHCID 5462224—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19040924HCID 190409244.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569664
Source datasetuspto-grants-1996_10
ORD IDord-0b4dfeb2292242cbbc852add7b738d1a
Source noteuspto-grants-1996_10