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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751264Generated: October 28, 2026

4-Fluorobenzaldehyde → HCID 58339529, compound

https://huagongshe.com/reaction/1751264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66658264HCID 66658264—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58339529HCID 5833952972.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

(2R,3S)-3-Amino-bicyclo[2,2,2]octane-2-carboxylic acid methyl ester hydrochloride (0.34 g, 1.54 mmol) was dissolved in methanol (10 mL). Sodium acetate (0.25 g, 3.08 mmol) was added followed by 4 Å powdered molecular sieves (0.34 g) and 4-fluoro-benzaldehyde (0.16 mL, 1.54 mmol). Sodium cyanoborohydride (0.19 g, 3.08 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 (20 mL) and ethyl acetate (30 mL). After shaking, both layers were passed through a plug of Celite. The organic layer was further washed with saturated aqueous sodium bicarbonate solution (10 mL), saturated aqueous brine solution (10 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the crude product, (2R,3S)-3-(4-fluoro-benzylamino)-bicyclo[2,2,2]octane-2-carboxylic acid methyl ester (0.32 g, 1.11 mmol, 72%), as a clear oil. LC-MS (ESI) calcd for C17H22FNO2 291.36, found 292.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156832B2
Source datasetuspto-grants-2015_10
ORD IDord-d092c4e1e4aa43b1b7f1dbdf97e4b52a
Source noteuspto-grants-2015_10