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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182405Generated: October 26, 2026

Triethylamine → N,N'-bis[(1S)-(2-naphthyl)-2-hydroxy-2-methylpropyl]-2,2-dimethylpropane-1,3-diamide

https://huagongshe.com/reaction/1182405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylmalonyl DichlorideHCID 4523180—
Reactant(S)-1-amino-1-(2-naphthyl)-2-methyl-2-propanolHCID 66807919—
SolventDichloromethaneHCID 6344—
ProductN,N'-bis[(1S)-(2-naphthyl)-2-hydroxy-2-methylpropyl]-2,2-dimethylpropane-1,3-diamideHCID 66807932100%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Under a nitrogen atmosphere, 1.5 g of (S)-1-amino-1-(2-naphthyl)-2-methyl-2-propanol, 0.84 g of triethylamine (dehydrated), and 13 mL of dichloromethane (dehydrated) were mixed and then cooled to an inner temperature of −10° C. 0.6 g of dimethylmalonic acid dichloride was added dropwise thereto over 3 minutes. The resulting mixture was warmed to room temperature. The mixture was stirred as such for 7 hours to effect reaction. After completion of the reaction, 20 mL of an aqueous saturated ammonium chloride solution was added thereto to separate into layers. The organic layer obtained was washed three times with 25 mL of water and concentrated. The concentrated residue was dried under reduced pressure at an inner temperature of 40° C. to obtain 1.8 g of N,N′-bis[(1S)-(2-naphthyl)-2-hydroxy-2-methylpropyl]-2,2-dimethylpropane-1,3-diamide (yield: 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288674B2
Source datasetuspto-grants-2007_10
ORD IDord-3c8cdc2353ad4d05872d5ded6fce08de
Source noteuspto-grants-2007_10