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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684441Generated: October 31, 2026

Water → HCID 131720052, compound

https://huagongshe.com/reaction/1684441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantSodium BicarbonateHCID 516892—
ReactantBoc-Trp(For)-OHHCID 7017963—
ProductHCID 131720052HCID 13172005247.7%

Reaction Steps

In 5 mg of DMP was dissolved 0.33 g of t-Boc-Trp(CHO)-OH, 0.17 g of sodium hydrogen carbonate was added. The solution was then stirred. To the mixture was added 1.08 g (5 mmol) of p-nitrobenzyl bromide, and stirring was effected at room temperature for 24 hours. Water and ethyl acetate were added to the reaction solution. The mixture was shaken, and the organic layer was recovered and the solvent was evaporated. The residue was purified with a silica gel column (manufactured by Merck Co., Kieselgel 60, 50 g, elution with hexane:ethyl acetate=6:4), to obtain 0.2 g of t-Boc-Trp(CHO)-OBzl (NO2). The peptide was dissolved in 5 ml of DMF, 0.5 ml of piperidine was added thereto, and the mixture was stirred at 0° C. for 1.5 hours. The solvent was evaporated under reduced pressure, 0.5 ml of 98% formic acid was added thereto, and the mixture was stirred at room temperature for 4 hours. About 30 ml of ether was added to obtain a precipitate. The precipitate was filtered and dried to obtain 0.16 g of H-Trp-OBzl (NO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639860
Source datasetuspto-grants-1997_06
ORD IDord-d6d4b7f9b74a4ba884e431cc7e7590f4
Source noteuspto-grants-1997_06