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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095263Generated: October 25, 2026

Triethylamine → N-dodecyl-2-carbobenzyloxyaminosuccinamic acid

https://huagongshe.com/reaction/1095263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDodecylamineHCID 13583—
Reactant(S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamateHCID 11128682—
SolventDichloromethaneHCID 6344—
ProductN-dodecyl-2-carbobenzyloxyaminosuccinamic acidHCID 5792548397%

Reaction Steps

N-Carbobenzyloxy-L-aspartic anhydride (1 mmol) was dissolved in 50 mL methylene chloride, followed by the addition of 1.05 eq of dodecylamine and 1.1 eq of triethylamine. The reaction was capped to prevent evaporation, and stirred for 12 hours. When no trace of starting material could be detected by thin layer chromatography (TLC) (CH2Cl2, 5% MeOH), the reaction was quenched with 20 mL 1N hydrochloric acid followed by extraction with chloroform (5×). The organic layer was dried over magnesium sulfate, and 7 was obtained as a white solid (yield 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138140B2
Source datasetuspto-grants-2012_03
ORD IDord-1401b6324ffe4ff991b4303fe3180ae7
Source noteuspto-grants-2012_03