Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814812Generated: November 1, 2026

DL-alanine → N-Butyrylalanine

https://huagongshe.com/reaction/1814812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDL-alanineHCID 602—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-ButyrylalanineHCID 11194480—

Reaction Conditions

Temperature0 °C

Reaction Steps

22.27 g (250 mmol) of D,L-alanine and 55.66 g (550 mmol) of triethylamine are dissolved in 250 ml of dichloromethane, and the solution is cooled to 0° C. 59.75 g (550 mmol) of trimethylsilyl chloride are added dropwise, and the solution is stirred at room temperature for 1 hour and at 40° C. for one hour. After cooling to −10° C., 26.64 g (250 mmol) of butyryl chloride are added dropwise, and the resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour. With ice-cooling, 125 ml of water are added dropwise, and the reaction mixture is stirred at room temperature for 15 minutes. The aqueous phase is evaporated to dryness, the residue is triturated with acetone and the mother liquor is filtered off with suction. Following removal of the solvent, the residue is chromatographed. The resulting product is dissolved in 3N aqueous sodium hydroxide solution, and the resulting solution is evaporated to dryness. The residue is taken up in conc. HCl and again evaporated to dryness. The residue is triturated with acetone, the precipitated solid is filtered off with suction and the solvent is removed under reduced pressure. This gives 28.2 g (71%) of a viscous oil which crystallizes after some time.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878708B2
Source datasetuspto-grants-2005_04
ORD IDord-31e1d85d8b2c4f0e93d8ab303bc7e3a9
Source noteuspto-grants-2005_04