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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857456Generated: November 3, 2026

Acetic Acid → HCID 86755976, compound

https://huagongshe.com/reaction/1857456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 69700361HCID 69700361—
Solvent1,2-DichloroethaneHCID 11—
SolventChloroformHCID 6212—
ProductHCID 86755976HCID 8675597646.8%

Reaction Steps

To a solution of cis-4-amino-2-methyl-2,3,4,6,7,8-hexahydro-cyclopenta[g]quinoline-1-carboxylic acid ethyl ester (Example 3) (0.35 g, 1.28 mmol) in anhydrous 1,2-dichloroethane (50 mL) was added acetic acid (0.73 mL, 1.28 mmol), followed by 3,5-bis(trifluoromethyl)benzaldehyde (0.21 mL, 1.28 mmol) and sodium triacetoxyborohydride (0.406 g, 1.92 mmol). The reaction was stirred at room temperature for 18 h. The reaction mixture was then diluted with chloroform and washed with 1 N NaOH. The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by silica gel chromatography using 10% ethyl acetate/hexanes as eluent afforded the title compound (approximately 300 mg). 1H NMR (CDCl3) δ1.1 (d, 3H), 1.3 (t, 3H), 2.6 (m, 1H), 3.6 (dd, 1H), 4.5 (m, 1H), 7.30 (s, 1H), 7.35 (s, 1H), 7.8 (s, 1H), 8.0 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147089
Source datasetuspto-grants-2000_11
ORD IDord-cd5212d1e53348ed8bef3aa42172bebd
Source noteuspto-grants-2000_11