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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268163Generated: November 2, 2026

Trifluoroacetic acid → HCID 69952803, compound

https://huagongshe.com/reaction/2268163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
Reactant1-Piperidinecarboxylic acid, 4-(2-(1,2-benzisoxazol-3-yl)ethyl)-, 1,1-dimethylethyl esterHCID 10019550—
SolventDichloromethaneHCID 6344—
ProductHCID 69952803HCID 6995280373%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326382B1
Source datasetuspto-grants-2001_12
ORD IDord-0086f865c069466b87d99b71e56f727e
Source noteuspto-grants-2001_12