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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168872Generated: October 31, 2026

Trifluoroacetic acid → HCID 22560655, compound

https://huagongshe.com/reaction/1168872

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 numberUS06627644B2
Source datasetuspto-grants-2003_09
ORD IDord-fe87b81a362d4bd8bbde46dac106ba64
Source noteuspto-grants-2003_09