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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424211Generated: October 29, 2026

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

https://huagongshe.com/reaction/424211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant3,4-DifluorobenzaldehydeHCID 588088—
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-(3,4-difluoro-benzylamino)-bicyclo[2.2.1]heptane-2-carboxylateHCID 6667477178%

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, 1.58 mmol) was dissolved in methanol (8 mL). Sodium acetate (0.26 g, 3.16 mmol) was added followed by 4 Å powdered molecular sieves (0.33 g) and 3,4-difluoro benzaldehyde (0.17 mL, 1.58 mmol). Sodium cyanoborohydride (0.22 g, 3.16 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-(3,4-difluoro-benzylamino)-bicyclo[2.2.1]heptane-2-carboxylate (0.36 g, 1.22 mmol, 78%), as a clear oil. LC-MS (ESI) calcd for C16H19F2NO2 295.32, found 296.3 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101800B2
Source datasetuspto-grants-2012_01
ORD IDord-77a76baa439b4996854d0cc70d7a06a4
Source noteuspto-grants-2012_01