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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548317Generated: October 29, 2026

Sodium Bicarbonate → methyl (1S,2R,3S,4R)-3-(4-fluoro-3-methyl-benzylamino)-bicyclo[2.2.1]heptane-2-carboxylate

https://huagongshe.com/reaction/548317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant4-Fluoro-3-methylbenzaldehydeHCID 2734874—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl (1S,2R,3S,4R)-3-aminobicyclo[2.2.1]heptane-2-carboxylate HydrochlorideHCID 66674231—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Productmethyl (1S,2R,3S,4R)-3-(4-fluoro-3-methyl-benzylamino)-bicyclo[2.2.1]heptane-2-carboxylateHCID 6667490777%

Reaction Conditions

Temperature25 °C

Reaction Steps

Methyl (1S,2R,3S,4R)-3-aminobicyclo[2.2.1]heptane-2-carboxylate hydrochloride (prepared as described in Example 6c, 0.32 g, 1.56 mmol) was dissolved in methanol (8 mL). Sodium acetate (0.26 g, 3.12 mmol) was added followed by 4 Å powdered molecular sieves (0.32 g) and 4-fluoro-3-methyl benzaldehyde (0.19 mL, 1.56 mmol). Sodium cyanoborohydride (0.24 g, 3.12 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, methyl (1S,2R,3S,4R)-3-(4-fluoro-3-methyl-benzylamino)-bicyclo[2.2.1]heptane-2-carboxylate (0.35 g, 1.20 mmol, 77%), as a clear oil. LC-MS (ESI) calcd for C17H22FNO2 291.36, found 292.5 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939524B2
Source datasetuspto-grants-2011_05
ORD IDord-395f5b0641134b7d984fa804fd2510de
Source noteuspto-grants-2011_05