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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731278Generated: October 30, 2026

4-Fluorobenzaldehyde → HCID 69062137, compound

https://huagongshe.com/reaction/731278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant142035-03-8HCID 69060013—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 69062137HCID 69062137316.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

The crude cis-2-amino-cyclohex-3-enecarboxylic acid methyl ester hydrochloride (2.8 mmol) was dissolved in methanol (5 mL). 4-Fluoro-benzaldehyde (37.3 mg, 0.3 mmol) was added, followed by 4 Å molecular sieves (0.5 g) and sodium acetate (0.46 g, 5.6 mmol). After stirring at 25° C. for 15 min, sodium cyanoborohydride (0.37 g, 5.9 mmol) was added and the mixture was stirred at 25° C. for 16 h. The mixture was poured into a mixture of saturated aqueous sodium bicarbonate solution (100 mL) and ethyl acetate (200 mL). After shaking, both layers were passed through a plug of Celite. The organic layer was washed with saturated aqueous sodium bicarbonate solution (100 mL), followed by saturated aqueous brine solution (100 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the crude product, cis-2-(4-fluoro-benzylamino)-cyclohex-3-enecarboxylic acid methyl ester (250 mg, 0.95 mmol, 34%), as a clear oil. LC-MS (ESI) calcd for C15H18FNO2 263.13, found 264.04 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-0a8881b70ed2462f8a6402fe9b05c12b
Source noteuspto-grants-2009_09