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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909878Generated: November 3, 2026

Triethylamine → (R)-N-(2,2-dimethoxyethyl)pentan-2-amine

https://huagongshe.com/reaction/909878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetaldehyde, 2,2-dimethoxy-HCID 162650—
Reactant(2R)-pentan-2-amine hydrochlorideHCID 86641258—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(R)-N-(2,2-dimethoxyethyl)pentan-2-amineHCID 59290396—

Reaction Steps

2,2-Dimethoxyacetaldehyde (0.59 mL) was added to a solution of (R)-pentan-2-amine hydrochloride (0.48 g) and triethylamine (0.54 mL) in methanol (4 mL) and the mixture stirred for 2 h. A slurry of palladium on carbon (10%, 20 mg) in methanol (1 mL) was added and the mixture hydrogenated at 5 bar for 20 h. The mixture was then filtered and in vacuo. The resulting residue was triturated with diethyl ether (5 mL) and the resulting white solid extracted with further diethyl ether (2×5 mL). The combined ether fractions were concentrated in vacuo to afford (R)—N-(2,2-dimethoxyethyl)pentan-2-amine (0.745 g) as an oil. 1H NMR (400 MHz, CDCl3) δ 4.92 (t, J=5.4 Hz, 1H), 3.47 (s, 3H), 3.47 (s, 3H), 3.25-3.15 (m, 1H), 2.99 (ddd, J=27.9, 12.7, 5.5 Hz, 2H), 1.86-1.77 (m, 1H), 1.64-1.54 (m, 1H), 1.49-1.32 (m, 5H), 0.95 (t, J=7.3 Hz, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017602B2
Source datasetuspto-grants-2011_09
ORD IDord-9796064ded7d41839f1826af1cff3fc5
Source noteuspto-grants-2011_09