HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066852Generated: October 31, 2026
Trifluoroacetic acid → 3-[2-(2-Fluoro-5-bromobenzyloxy)ethyl]piperidine
https://huagongshe.com/reaction/1066852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-(t-Butoxycarbonyl)-3-[2-(2-fluoro-5-bromobenzyloxy)ethyl]piperidine | HCID 21196136 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[2-(2-Fluoro-5-bromobenzyloxy)ethyl]piperidine | HCID 21196120 | — |
Reaction Steps
In a 1-ml round bottom flask 1-(t-butoxycarbonyl)-3-[2-(2-fluoro-5-bromobenzyloxy)ethyl]piperidine (0.495 g) was dissolved in methylene chloride (4 ml) under a nitrogen atmosphere. The solution was cooled to 0° C. and trifluoroacetic acid (1 ml) was slowly added dropwise. The resulting mixture was stirred for thirty minutes at ambient temperature. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The resulting residue was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245761B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-66e0ef759dcc42a28d4664241a88bf9b |
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| Source note | uspto-grants-2001_06 |
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