Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918554Generated: October 27, 2026

Hydrochloric Acid → (S)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid

https://huagongshe.com/reaction/1918554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantEthoxalyl chlorideHCID 20884—
Reactantphenylalaninol, (S)-HCID 447213—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acidHCID 6683189194%

Reaction Steps

Triethylamine (0.703 mL; 5.01 mmol) was added to the mixture of (S)-2-amino-3-phenylpropan-1-ol (0.515 g; 3.34 mmol) and ethyl 2-chloro-2-oxoacetate (0.400 mL; 3.50 mmol) in dichloromethane (15 mL) at 0° C. After addition, the mixture was stirred at room temperature for 30 minutes, diluted with 40 mL of dichloromethane, and washed successively with an aqueous solution of sodium carbonate, and water. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. Water (5 mL) and a 2M solution of sodium hydroxide (5 mL; 10 mmol) were added to the resulting residue and the mixture was stirred at room temperature for 10 minutes. Water (10 mL) was added and the pH of the solution was adjusted to 1 by addition of a 6N hydrochloric acid. The formed solid was filtered off, and the filtrate was extracted with ethyl acetate (5×20 mL). The combined organic layers were dried over magnesium sulfate and evaporated to dryness to give 0.692 g (94%) of (S)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-266b55f26e974384a9305613b48a5206
Source noteuspto-grants-2013_12