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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413346Generated: November 1, 2026

Triethylamine → HCID 20291877, compound

https://huagongshe.com/reaction/1413346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
Reactant6-(4-Nitro-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acidHCID 303582—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 20291877HCID 2029187794%

Reaction Conditions

Temperature50 °C

Reaction Steps

2.58 ml (0.018 mol) of triethylamine, followed by 1.3 g (0.0198 mol) of sodium azide, are added to a mixture of 5.7 g (0.018 mol) of 6-(3-nitrophthalimidyl)-caproic acid in 35 ml of dimethylsulphoxide. The reaction mixture is heated for 6 hours at 50° C. and is then concentrated in vacuo, diluted with 100 ml of water and acidified with 4 ml of concentrated hydrochloric acid. The resulting suspension of the reaction product is stirred for 18 hours and filtered with suction, and the filter residue is washed with 20 ml of water and dried for 24 hours at 60° C./0.100. mm Hg, over phosphorus pentoxide. 5.1 g (94% of theory) of 6-(3-azidophthalimidyl)-caproic acid are obtained; melting point 87°-90° C. (with decomposition). IR spectrum (CH2Cl2): 1780 and 1725 cm-1 (CO--N--CO); 2130 cm-1 (N3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250096
Source datasetuspto-grants-1981_02
ORD IDord-b3148f537cf5496c8ccd06d8e655dec5
Source noteuspto-grants-1981_02