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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711813Generated: October 26, 2026

Methylamine → Methyl-(1-propyl-naphthalen-2-ylmethyl)amine

https://huagongshe.com/reaction/1711813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1-Propyl-naphthalene-2-carbaldehydeHCID 1201452—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl-(1-propyl-naphthalen-2-ylmethyl)amineHCID 5945695989%

Reaction Steps

A solution of 2.0 M methylamine in methanol (20 mL) was added to 1-propyl-naphthalene-2-carbaldehyde (0.983 g, 4.95 mmol) under N2 and allowed to stir for 18 h. The solution was concentrated under reduced pressure. Then the resulting dark yellow oil was solvated in EtOH (20 mL) under N2. To the solution was added NaBH4 (0.187 g, 4.95 mmol) and the mixture allowed to stir for 6.5 h. The reaction was concentrated under reduced pressure, then solvated in 1 N NaOH (20 mL) and extracted with Et2O (3×50 mL). The organics were combined, washed with brine (2×100 mL), dried over Na2SO4, filtered and concentrated to yield the title compound (0.94 g, 89%) as a yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 7.87-7.73 (m, 4H), 7.51-7.43 (m, 3H), 3.53 (m, 1H), 2.09 (s, 3H), 1.70-1.52 (m, 2H), 1.26-1.12 (m, 2H), 0.87-0.79 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-9905f4eb812845868f910e505b9d6b6b
Source noteuspto-grants-2010_09