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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911765Generated: November 1, 2026

Acetic Acid → HCID 58689747, compound

https://huagongshe.com/reaction/1911765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58689760HCID 58689760—
SolventMethanolHCID 887—
ProductHCID 58689747HCID 5868974770.6%

Reaction Steps

To a solution of 3,5-bis-trifluoromethyl benzaldehyde (0.185 g, 0.76 mmol) in MeOH (3 mL) was added (3-aminomethyl-5,6,7,8-tetrahydro-quinoline-2-yl)-cyclopentylmethyl-ethylamine (0.2 g, 0.69 mmol), followed by the addition of acetic acid (0.08 mL, 1.39 mmol). This reaction mixture was stirred at RT for 1 h, after which time sodium cyanoborohydride (0.172 g, 2.78 mmol) was added, and stirring was continued for another 8 h. The solvent was then evaporated under vacuum and water was added, followed by extraction of the product with ethyl acetate. The organic layer was washed with saturated sodium bisulfite solution, the organic layer was separated and dried over sodium sulfate, and the solvent was evaporated to give the {3-[(3,5-bis-trifluoromethyl-benzylamino)-methyl]-5,6,7,8-tetrahydro-quinolin-2-yl}-cyclopentylmethyl-ethylamine (0.250 g, yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604055B2
Source datasetuspto-grants-2013_12
ORD IDord-f3cad4f620a64133bea8dbedd53089d7
Source noteuspto-grants-2013_12