HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81158Generated: November 2, 2026
Benzaldehyde → (2R,3R)-3-(benzylamino)pentan-2-ol
https://huagongshe.com/reaction/81158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (2R,3R)-3-aminopentan-2-ol hydrochloride | HCID 90236209 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2R,3R)-3-(benzylamino)pentan-2-ol | HCID 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 APCl calc'd for C12H19NO [M+H]+ 194. found 194.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846657B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-d8714113189b44da95a201fdeadf34c1 |
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| Source note | uspto-grants-2014_09 |
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