HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068434Generated: October 30, 2026
1-(Bromomethyl)-3-(trifluoromethoxy)benzene → HCID 54425085, compound
https://huagongshe.com/reaction/1068434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Bromomethyl)-3-(trifluoromethoxy)benzene | HCID 737176 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylate | HCID 2758812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54425085 | HCID 54425085 | — |
Reaction Steps
To a cold (−78° C.) solution of ethyl N-tert-butoxycarbonylpiperidine-4-carboxylate (5.16 g, 20.05 mmol) in anhydrous tetrahydrofuran (60 mL), a solution of sodium bis(trimethylsilyl)amide (28 mL, 1M, 28 mmol) was added over a period of 30 min. The resultant mixture was stirred at −78° C. for 1 h, and 3-(trifluoromethoxy)benzyl bromide (5.90 g, 23.14 mmol) was added. The reacting mixture was allowed to warm to room temp. and stirred overnight. The product mixture was concentrated, and the residue was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 20% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248756B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-e63540c3adaf4927bca38732387e2492 |
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| Source note | uspto-grants-2001_06 |
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