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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195136Generated: October 30, 2026

p-Toluenesulfonic acid → 3-[[(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-1-oxo-3-phenylpropyl]amino]propanoic acid, phenylmethyl ester

https://huagongshe.com/reaction/1195136

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
ReactantBenzyl 3-aminopropanoateHCID 1116164—
Solvent1,1-DichloroethaneHCID 6365—
Product3-[[(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-1-oxo-3-phenylpropyl]amino]propanoic acid, phenylmethyl esterHCID 1368620298%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.03 g of TEA was added to a mixture of 5.84 g of Boc-Phe-OH and 7.03 g of TosOH.β-Ala-OBzl in 80 ml of dichloroethane. 4.54 g of DCC was added to the solution at 0 ° C. After stirring for 3 hrs at 0 ° C. and overnight at room temperature, precipitated DCUrea was filtered off and the solvent was distilled in vacuo. The residue was dissolved in ethyl acetate and the solution was washed with 10% citric acid aqueous solution, water, 5% sodium hydrogencarbonate aqueous solution and brine. After dehydration over sodium sulfate anhydride, the solvent was evaporated to give 8.36 g of Boc-Phe-β-Ala-OBzl; yield 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110797
Source datasetuspto-grants-1992_05
ORD IDord-3a2a66bb0c7544188992b04270ad5310
Source noteuspto-grants-1992_05