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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822089Generated: November 1, 2026

N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide ester → HCID 131727693, compound

https://huagongshe.com/reaction/1822089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrobenzylamine hydrochlorideHCID 11252467—
SolventDichloromethaneHCID 6344—
ProductHCID 131727693HCID 131727693—

Reaction Steps

4-Nitrobenzylamine hydrochloride (1 g; 5.3 mmol) and diisopropylethylamine (1.8 ml; 10.6 mmol) were dissolved in 70 ml of dichloromethane at RT. BOC-Gly-OSu (1.44 g; 5.3 mmol) was added and the solution was stirred at RT overnight. After evaporating the solvent in a rotary evaporator, the residue was taken up in 50 ml of ethyl acetate and extracted in each case 2× with 5% KHSO4, 5% NaHCO3 and distilled water. The organic phase was dried over Na2SO4, the solvent was evaporated and toluene was then added and evaporated in a rotary evaporator. The resultant oil was dissolved, without further work-up, directly in 15 ml of 4M HCl/dioxane and stirred at RT. After a short time, the product starts to precipitate. After 1 h, the solvent was evaporated, the solid was suspended in 100 ml of ethyl acetate, filtered off and washed with petroleum ether. The white solid was dried under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608623B2
Source datasetuspto-grants-2009_10
ORD IDord-bb38a4c5846c4666870424f2503fb21b
Source noteuspto-grants-2009_10