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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11254Generated: October 25, 2026

Chlorotrimethylsilane → 2-Butyrylaminobutyric acid

https://huagongshe.com/reaction/11254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAlpha-Aminobutyric AcidHCID 6657—
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Butyrylaminobutyric acidHCID 12408866—

Reaction Conditions

Temperature0 °C

Reaction Steps

25.78 g of 2-aminobutyric acid (250 mmol) 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. Aqueous sodium hydroxide solution is added to the organic phase, and the organic solvent is removed under reduced pressure. The residue is acidified and the precipitated solid is triturated once with water and twice with petroleum ether and dried under reduced pressure at 45° C. 29.1 g (67%) of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098207B2
Source datasetuspto-grants-2006_08
ORD IDord-46b5a06419784ab4aa0ab701d258a09a
Source noteuspto-grants-2006_08