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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884270Generated: October 29, 2026

4-Fluorobenzaldehyde → rac-Methyl (1R,2R,4S,5S,65,7R)-7-{[(4-fluorophenyl)methyl]amino}tricyclo[3.2.2.02,4]nonane-6-carboxylate

https://huagongshe.com/reaction/884270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactantrac-Methyl (1R,2R,4S,5S,6S,7R)-7-aminotricyclo [3.2.2.02,4]nonane-6-carboxylate hydrochlorideHCID 131728832—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Productrac-Methyl (1R,2R,4S,5S,65,7R)-7-{[(4-fluorophenyl)methyl]amino}tricyclo[3.2.2.02,4]nonane-6-carboxylateHCID 123318675—

Reaction Conditions

Temperature25 °C

Reaction Steps

rac-Methyl (1R,2R,4S,5S,6S,7R)-7-aminotricyclo[3.2.2.02,4]nonane-6-carboxylate hydrochloride (0.43 g, 1.85 mmol) was dissolved in methanol (10 mL). Sodium acetate (0.30 g, 3.70 mmol) was added followed by 4 Å powdered molecular sieves (0.40 g) and 4-fluoro-benzaldehyde (0.20 mL, 1.85 mmol). Sodium cyanoborohydride (0.23 g, 3.70 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, rac-Methyl (1R,2R,4S,5S,65,7R)-7-{[(4-fluorophenyl)methyl]amino}tricyclo[3.2.2.02,4]nonane-6-carboxylate 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 numberUS08236948B2
Source datasetuspto-grants-2012_08
ORD IDord-970fbb0f68664d65993d883bc3c52de3
Source noteuspto-grants-2012_08