HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51199Generated: October 26, 2026
Methanol → 1,6-Hexanediyl dianthranilate
https://huagongshe.com/reaction/51199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 1,6-Hexanediol | HCID 12374 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,6-Hexanediyl dianthranilate | HCID 86590777 | 78% |
Reaction Steps
A mixture of 1,6-hexanediol (118 grams, 1.0 mol; obtained from Sigma-Aldrich), isatoic anhydride (367 grams, 2.25 mol), and 1,4-diazabicyclo[2.2.2]octane (22.4 grams, 0.20 mol) in 500 milliliters of dimethyl formamide in a 4 liter beaker was heated at 120° C. for 1.5 hours. The mixture was then cooled to room temperature and was stirred as first methanol (1,500 milliliters) and then water (750 milliliters) were added. The resultant suspension was stirred for 2 hours, and then was filtered. The solid was washed in the filter funnel with 2×200 milliliter portions of 75:25 methanol/water, then with 250 milliliters of water, and again with 2×200 milliliter portions of 75:25 methanol/water. Drying in the air for 72 hours gave the desired 1,6-hexanediyl dianthranilate product as a light beige solid (277.5 grams, 78 percent yield). A 1H-NMR spectrum indicated that the product was highly pure (greater than 98 percent). The melting point of this product as measured by Differential Scanning Calorimetry was 78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713614B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-963bed18cac149169ca1c9bf22997171 |
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| Source note | uspto-grants-2004_03 |
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