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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218082Generated: October 27, 2026

Sodium Bicarbonate → 1-(Benzyl-methyl-amino)-heptan-3-one

https://huagongshe.com/reaction/2218082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-(benzyl-methyl-amino)-N-methoxy-N-methyl-propionamideHCID 59769556—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(Benzyl-methyl-amino)-heptan-3-oneHCID 1798192281%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Add butyllithium (12.3 ml (1.6 M solution in hexane), 19.6 mmol) to a stirred solution of 3-(benzyl-methyl-amino)-N-methoxy-N-methyl-propionamide and anhydrous tetrahydrofuran (70 ml) at −40° C. under N2. Stir for 1 hr at −40° C. Quench the reaction with saturated ammonium chloride (25 ml), allow the reaction to reach room temperature and add saturated sodium bicarbonate. Extract with ethyl acetate, wash with brine and dry over sodium sulfate. Filter off and concentrate to give the crude product. Purify the compound by flash chromatography, eluting with 2% ethanol/0.2% ammonium hydroxide/chloroform to yield 2.41 g (81%) of 1-(benzyl-methyl-amino)-heptan-3-one: mass spectrum (ion spray) m/z=234 (M+1); 1H NMR (CDCl3) δ 7.31-7.24 (m, 5H), 3.5 (s, 2H), 2.74-2.7 (m, 2H), 2.64-2.60 (m, 2H), 2.41 (t, 2H), 2.19 (s, 3), 1.59-1.51 (m, 2H), 1.35-1.28 (m, 2H), 0.91 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410982B2
Source datasetuspto-grants-2008_08
ORD IDord-ec4b7a7c87f24eefa2e9a06de9aa68b2
Source noteuspto-grants-2008_08