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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751238Generated: October 28, 2026

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

https://huagongshe.com/reaction/1751238

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 numberUS09156832B2
Source datasetuspto-grants-2015_10
ORD IDord-56bc2e5de8fa4661b3f281a77d11f480
Source noteuspto-grants-2015_10