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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457183Generated: October 27, 2026

Acetaldehyde → Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/457183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductTert-butyl 3-(ethylamino)pyrrolidine-1-carboxylateHCID 20800658—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (R)-3-amino-1-N-Boc pyrrolidine (1 eq, 5.37 mmol) in methanol (20 mL) was added acetaldehyde (0.95 eq) and the resulting mixture was heated to 80° C. and stirred for 2 h., then stirred at room temperature overnight. Sodium borohydride (0.95 eq, 5.1 mmol) was added and reaction mixture was stirred for an additional 2 h. The reaction mixture was concentrated, dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using hexane/ethyl acetate (10%) to hexane/ethyl acetate (50%). 1H-NMR (CDCL3) δ: 1.05 (3H, t), 1.45 (9H, s), 1.60–1.75 (1H, m), 2.00–2.10 (1H, m), 2.68 (4H, q), 2.90–3.15 (1H, m), 3.25–3.65 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-a16406f65fbb4f5eb39f97d477e53381
Source noteuspto-grants-2007_03