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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,4-Dioxane-2,6-dione | HCID 78232 | — |
| Reactant | 1-Amino-11-azido-3,6,9-trioxaundecane | HCID 2735280 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Azido-13-oxo-3,6,9,15-tetraoxa-12-azaheptadecan-17-oic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608243B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-b6d799394eca4955868e222f3bc15ce3 |
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| Source note | uspto-grants-2009_10 |
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