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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983465Generated: October 30, 2026

Trifluoroacetic acid → HCID 22560655, compound

https://huagongshe.com/reaction/983465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69745654HCID 69745654—
SolventDichloromethaneHCID 6344—
ProductHCID 22560655HCID 22560655112.3%

Reaction Steps

To a solution of 4-{[(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-methyl}-piperidine-1-carboxylic acid tert-butyl ester (2.4 g, 4.56 mmol) in methylene chloride (30 mL) under a nitrogen atmosphere was added trifluoroacetic acid (10 mL). The reaction was stirred at room temperature for 30 min. and concentrated in vacuo. The residue was partitioned between EtOAc (50 mL) and 10% aq. KOH (50 mL). The organic layer was separated, dried over MgSO4, filtered, and concentrated to afford (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-piperidin-4-ylmethyl-propyl-amine (1.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864266B2
Source datasetuspto-grants-2005_03
ORD IDord-1a1148e656d24ce19d10adda8ed66c2b
Source noteuspto-grants-2005_03