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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172391Generated: November 2, 2026

Acetic Acid → [1-(4-Fluoro-benzylamino)-cyclopentyl]-acetic acid methyl ester

https://huagongshe.com/reaction/1172391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 1-aminocyclopentaneacetateHCID 57446164—
SolventMethanolHCID 887—
SolventSodium BicarbonateHCID 516892—
Product[1-(4-Fluoro-benzylamino)-cyclopentyl]-acetic acid methyl esterHCID 5760659750.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (1-amino-cyclopentyl)-acetic acid methyl ester (318 mg, 2.02 mmol) in anhydrous methanol (10 mL) was treated with 4-fluoro-benzaldehyde (0.27 mL, 2.56 mmol) and stirred at 25° C. under a nitrogen environment. After 10 min, glacial acetic acid (0.384 mL, 6.71 mmol) and sodium triacetoxyborohydride (1.1 g, 5.05 mmol) were added sequentially, and the resulting mixture was stirred at 25° C. for 18 h. The reaction was diluted with a saturated aqueous sodium bicarbonate solution (20 mL) and extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with brine (20 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to give [1-(4-fluoro-benzylamino)-cyclopentyl]-acetic acid methyl ester (270 mg, 50%) as a colorless oil. LC-MS (ESI) calculated for C15H20FNO2: 265.3, found 266.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834009B2
Source datasetuspto-grants-2010_11
ORD IDord-604010e13b0243edb0c0afd90d686099
Source noteuspto-grants-2010_11