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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111923Generated: November 1, 2026

Trifluoroacetic acid → HCID 57640339, compound

https://huagongshe.com/reaction/2111923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68575168HCID 68575168—
SolventDichloromethaneHCID 6344—
ProductHCID 57640339HCID 5764033987.8%

Reaction Steps

Trifluoroacetic acid (15 ml, 195 mmol) is added to a solution of 4-{[(benzofuran-2-yl)methyl]-(3-methylbutyl)-amino}-piperidine-1-carboxylic acid tert-butyl ester (1.17 g, 2.92 mmol) in dichloromethane (15 ml). The reaction is stirred overnight at room temperature. The reaction is concentrated and water added to the residue. The solution is loaded onto a SCX-2 (10 g) column and washed with water (20 ml) and methanol (20 ml). The product is then eluted off with 2M ammonia in methanol (30 ml) and concentrated on a rotary evaporator to yield (0.77 g) of N-(3-methylbutyl)-N-[(benzofuran-2-yl)methyl]piperidin-4-amine: mass spectrum (ion spray): m/z=301 (M+1); 1H NMR (CDCl3): δ=7.52-7.43 (2H, m), 7.25-7.16 (2H, m), 6.56 (1H, s), 3.81 (2H, s), 3.14 (2H, brd), 2.72-2.52 (5H, m), 1.86-1.75 (3H, brm), 1.64-1.34 (5H, m), 0.92-0.83 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521462B2
Source datasetuspto-grants-2009_04
ORD IDord-98342db8b83c4dbe8c53245ef81ff0d4
Source noteuspto-grants-2009_04