HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268163Generated: November 2, 2026
Trifluoroacetic acid → HCID 69952803, compound
https://huagongshe.com/reaction/2268163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Piperidinecarboxylic acid, 4-(2-(1,2-benzisoxazol-3-yl)ethyl)-, 1,1-dimethylethyl ester | HCID 10019550 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69952803 | HCID 69952803 | 73% |
Reaction Steps
Trifluoroacetic acid (TFA) (7 mL) was added dropwise to a cold (0° C.) solution of the piperidine formed in step d (0.50 g, 1.51 mmol) in methylene chloride (7 mL). The resulting solution was stirred at 0° C. for 30 min. Volatiles were removed under reduced pressure and excess TFA was removed by concentrating from toluene twice. The crude product was redissolved in methylene chloride (10 mL) and then triethylamine (0.42 mL, 3.01 mmol) and benzyl bromide (0.18 mL, 1.51 mmol) were added. The resulting mixture was stirred overnight (15 hours) at room temperature. The mixture was washed with water and brine and dried (MgSO4), filtered, and concentrated. Purification by silica gel flash chromatography (50% ethyl acetate/hexanes) gave the title compound (free base) (0.350 g, 73%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06326382B1 |
|---|
| Source dataset | uspto-grants-2001_12 |
|---|
| ORD ID | ord-0086f865c069466b87d99b71e56f727e |
|---|
| Source note | uspto-grants-2001_12 |
|---|