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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408813Generated: October 28, 2026

4-Fluorobenzaldehyde → HCID 66674915, compound

https://huagongshe.com/reaction/2408813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66673812HCID 66673812—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 66674915HCID 6667491587%

Reaction Conditions

Temperature25 °C

Reaction Steps

Methyl (1S,2S,3R,4R)-3-aminobicyclo[2.2.1]heptane-2-carboxylate hydrochloride (1 g, 4.86 mmol) was dissolved in methanol (23 mL). Sodium acetate (0.755 g, 9.2 mmol) was added followed by 4 Å powdered molecular sieves (1 g) and 4-fluoro-benzaldehyde (0.571 g, 4.6 mmol). Sodium cyanoborohydride (0.578 g, 9.2 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 (200 mL) and ethyl acetate (300 mL). After shaking, both layers were passed through a plug of Celite. The organic layer was further washed with saturated aqueous sodium bicarbonate solution (100 mL), saturated aqueous brine solution (100 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the crude product, methyl (1S,2S,3R,4R)-3-[(4-fluorobenzyl)amino]bicyclo[2.2.1]heptane-2-carboxylate (1.11 g, 4.0 mmol, 87%), as a clear oil. LC-MS (ESI) calcd for C16H20FNO2 277.15, found 278.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815847B2
Source datasetuspto-grants-2014_08
ORD IDord-0cdf401b8e4e435980456d9a600653e6
Source noteuspto-grants-2014_08