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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821549Generated: October 30, 2026

Water → 1-Azido-13-oxo-3,6,9,15-tetraoxa-12-azaheptadecan-17-oic acid

https://huagongshe.com/reaction/1821549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
Reactant1,4-Dioxane-2,6-dioneHCID 78232—
Reactant1-Amino-11-azido-3,6,9-trioxaundecaneHCID 2735280—
SolventDichloromethaneHCID 6344—
Product1-Azido-13-oxo-3,6,9,15-tetraoxa-12-azaheptadecan-17-oic acidHCID 71357990—

Reaction Steps

To a solution of 11-azido-3,6,9-trioxaundecanamine (10.9 g, 50.0 mmol) in dichloromethane (100 ml) was added diglycolic anhydride (6.38 g, 55.0 mmol). The reaction mixture was stirred overnight. HPLC analysis (column Vydac 218TP54; solvents: A=water/0.1% TFA and B═acetonitrile/0.1% TFA; gradient 4-16% B over 20 min; flow 1.0 ml/min; UV detection at 214 and 284 nm), showed complete conversion of starting material to a product with retention time 18.3 min. The solution was concentrated to give quantitative yield of a yellow syrup. The product was analysed by LC-MS (ES ionisation) giving [MH]+at 335 as expected. 1H (500 MHz) and 13C (125 MHz) NMR spectroscopy was in agreement with structure The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608243B2
Source datasetuspto-grants-2009_10
ORD IDord-b6d799394eca4955868e222f3bc15ce3
Source noteuspto-grants-2009_10