Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852766Generated: November 3, 2026

Benzaldehyde → (2R,3R)-3-(benzylamino)pentan-2-ol

https://huagongshe.com/reaction/1852766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(2R,3R)-3-aminopentan-2-ol hydrochlorideHCID 90236209—
SolventDichloromethaneHCID 6344—
Product(2R,3R)-3-(benzylamino)pentan-2-olHCID 86724514—

Reaction Steps

To a solution of (2R,3R)-3-aminopentan-2-ol hydrochloride (1.00 g, 7.2 mmol) in DCM (20 mL) at rt was added sodium bicarbonate solution (604 mg, 7.2 mmol dissolved in 3.0 mL of water), dropwise. The reaction mixture was stirred for 1 hour, and the solvent was evaporated under reduced pressure. The residue and sodium cyanoborohydride (600 mg, 10.7 mmol) were added to a solution of benzyaldehyde 877 mg, 8.6 mmol) in DCM (20 mL). The reaction mixture was stirred at room temperature overnight and then concentrated in vacuo. 30.0 mL water was added to this mixture, and the aqueous layer was extracted with dichloromethane (3×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes) afforded (2R,3R)-3-(benzylamino)pentan-2-ol. MS APCI calc'd for C12H19NO [M+H]+ 194. found 194.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962611B2
Source datasetuspto-grants-2015_02
ORD IDord-3acefd5ecaa44b4dae8b2ae5c7e94154
Source noteuspto-grants-2015_02