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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759763Generated: November 2, 2026

p-Toluenesulfonic acid → Boc-Gly-Phe-Gly-OBzl

https://huagongshe.com/reaction/1759763

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantPhe-Gly-OBzlHCID 91977316—
SolventDimethylformamideHCID 6228—
ProductBoc-Gly-Phe-Gly-OBzlHCID 13172286065.5%

Reaction Conditions

Temperature4 °C

Reaction Steps

A mixture of p-toluenesulfonic acid salt of Phe-Gly-OBzl (3.06 g), Boc-Gly-OH (1.10 g), N-hydroxysuccinimide (941 mg), N-methylmorpholine (0.725 ml), and N,N-dimethylformamide (40 ml) was cooled to 4° C., and added with N,N′-dicyclohexylcarbodiimide (1.56 g). The mixture was allowed to react overnight at room temperature with stirring, and then evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane:methanol=98:2 solution) to give Boc-Gly-Phe-Gly-OBzl (1.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838450B2
Source datasetuspto-grants-2005_01
ORD IDord-eb6c174252504210838604370a08b4ac
Source noteuspto-grants-2005_01