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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649899Generated: November 1, 2026

Triethylamine → 1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexane

https://huagongshe.com/reaction/1649899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-t-butoxycarbonyl-N-methylamino-2-hydroxy-5-methylhexaneHCID 19753986—
SolventDimethyl SulfoxideHCID 679—
Product1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexaneHCID 1975392588.5%

Reaction Steps

To a solution of 1-(N-t-butoxycarbonyl-N-methylamino)2-hydroxy-5-methylhexane (2.45 g) and triethylamine (3.03 g) in dimethyl sulfoxide (20 ml) was added sulfur trioxide pyridine complex (4.77 g) under ice-bath cooling. After the mixture was stirred at ambient temperature overnight, the reaction mixture was poured into ice-water (100 ml). The mixture was extracted with diethyl ether (100 ml×2). The extract was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (20% ethyl acetate in n-hexane as eluent) to give 1-(N-t-butoxycarbonyl-N-methylamino)-2-oxo-5-methylhexane (2.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921855
Source datasetuspto-grants-1990_05
ORD IDord-b4235977be334e6f93e4f37e03f885a3
Source noteuspto-grants-1990_05