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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884234Generated: November 1, 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/884234

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 numberUS08236948B2
Source datasetuspto-grants-2012_08
ORD IDord-d32618dfc8274df9b6862fc42ab59ff8
Source noteuspto-grants-2012_08