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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360719Generated: November 1, 2026

Acetic Acid → 1-naphthalenemethanamine, n,n-dimethyl-

https://huagongshe.com/reaction/2360719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-NaphthaldehydeHCID 6195—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium AcetateHCID 517045—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
Product1-naphthalenemethanamine, n,n-dimethyl-HCID 26495392%

Reaction Steps

To 1-naphthaldehyde (1.50 g, 9.62 mmol, 1.00 equiv) in 40 mL THF is added NaOAc (0.79 g, 9.62 mmol, 1.00 equiv), Me2NH.HCl (863 mg, 10.6 mmol, 1.10 equiv), and AcOH (0.11 mL, 1.9 mmol, 0.20 equiv) at 23° C. NaBH(OAc)3 (4.08 g, 19.3 mmol, 2.00 equiv) is added in three portions over five minutes. The suspension is stirred for 12 hours before solvent is removed in vacuo. To the residue is added 10 mL sat. NaHCO3(aq) and 10 mL CH2Cl2. The phases are separated and the aqueous phase is extracted with CH2Cl2 (3×10 mL). The combined organic phase is concentrated in vacuo. The residue is purified by chromatography on silica gel eluting with hexanes/EtOAc 3:2 (v/v) to afford 1.64 g of the title compound as a colorless liquid (92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686158B2
Source datasetuspto-grants-2014_04
ORD IDord-2fcfad24e6e447e4a4f3da52905adbaf
Source noteuspto-grants-2014_04