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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108867Generated: November 1, 2026

Hydrochloric Acid → HCID 69848410, compound

https://huagongshe.com/reaction/1108867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMalonic AcidHCID 867—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantPenicillin G PotassiumHCID 23664709—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductBenzeneacetamideHCID 7680—
ProductHCID 69848410HCID 6984841058%

Reaction Steps

Phenylacetamide intermediate AG3 was prepared using standard methods as shown in Scheme AG (E. Profft, J. Prakt. Chem. 1965, 30, 18). A mixture of AG1 (0.47 mol), EtOH (100 mL), NH4OAc (0.47 mol), and malonic acid (0.70 mol) was heated at reflux for 6 h, cooled, and filtered. The white solid was washed with EtOH and MeOH and dried. This solid was dissolved in 2:1 acetone/water (360 mL), treated with triethylamine (0.72 mol) and phenylacetyl chloride (0.36 mol), and stirred for 22 h. The mixture was evaporated and the residue dissolved in water (500 mL) and adjusted to pH 12 (1 N NaOH). The aqueous layer was adjusted to pH 2 (conc. HCl), extracted with Et2O, and evaporated to a white foam. The foam was purified by silica gel chromatography (10% MeOH/DCM) to give AG3. A solution of compound AG3 (0.22 mol) in water (600 mL) at RT was adjusted to pH 7.5 using KOH (3.0 N) and treated with penicillin amidase (91520 units, Sigma). This mixture was stirred for 47 h, acidified to pH 1 with HCl (conc), and the resultant ppt filtered through Celite. The filtrate was extracted with Et2O (3×300 mL), concentrated in vacuo, and treated with MeOH/conc. NH4OH (9:1). This product-containing solution was purified by silica gel chromatography (eluent DCM/MeOH/NH4OH, 78:18:4) to give (S)-3-phenylacetamido-3-(3-pyridyl)propionic acid ammonium salt (19.5 g, 58%). This product was treated with HCl (6.0 N, 292 mL), heated at reflux for 5 h, cooled to RT, and extracted with Et2O (3×200 mL). The aqueous layer was adjusted to pH 12, concentrated in vacuo, and the resultant solid triturated with MeOH (2×300 mL). This solution was evaporated to give ca. 14 g sodium salt. This material was treated with MeOH (500 mL), 2,2-dimethoxypropane (44 mL), and HCl (4 N in dioxane, 84 mL), and stirred for 90 h at RT. This mixture was filtered and the filtrate concentrated in vacuo. The resultant off-white solid was triturated with Et2O (2×150 mL) and dried to give compound AG5 (16.7 g, 96% ee) as a white, amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069254
Source datasetuspto-grants-2000_05
ORD IDord-ea4eae7d61984f9ea2ad01de21414ddf
Source noteuspto-grants-2000_05