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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263387Generated: October 30, 2026

Hydrochloric Acid → HCID 86751008, compound

https://huagongshe.com/reaction/263387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-PhenylalanineHCID 6140—
ReactantSodium HydroxideHCID 14798—
ReactantValine methyl esterHCID 94285—
ReactantTrimethylaluminumHCID 16682925—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 86751008HCID 8675100834%

Reaction Steps

A solution of trimethylaluminum (136.2 mL of a 2M solution in hexane, 272.4 mmol) was added dropwise to a stirring suspension of L-phenylalanine (15.0 g, 90.79 mmol) in 150 mL of methylene chloride at 0° C. (ice-bath). The resultant clear solution was allowed to warm to room temperature and stirred for 23 h. A solution of the free base of L-valine methyl ester (15.22 g, 90.79 mmol) in 100 mL of methylene chloride was added dropwise and the resultant clear solution was stirred at room temperature for 72 h. The reaction mixture was then cooled to 0° C. and with stirring, 6N HCl was dropwise until the pH was 2. The mixture was stirred for an additional 0.5 h followed by addition of 40 mL of 50% aqueous NaOH until the pH was 13. To this mixture was added 800 mL of methylene chloride and 100 mL of water. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure to provide a residue which was chromatographed on silica gel using 5% methanol in methylene chloride as the eluting solvent. The desired fractions were collected and evaporated under reduced pressure to yield 5.0 g (34%) of the title product as a colorless oil. IR (neat, cm-1), C=O (1665.8, 1742.0), N--H (3366.6). 1H NMR and 13C NMR (CDCl3) spectra were both consistent with the title product. Analysis calculated for C15H22ClN2Oe ·1/4H2O: C, 56.41; H, 7.42; N, 8.77; Cl, 11.10; Found: C, 56.34; H, 7.65; N, 8.61; Cl, 10.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643855
Source datasetuspto-grants-1997_07
ORD IDord-08f865fcca944c2fa39a4c1145185d99
Source noteuspto-grants-1997_07