HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158550Generated: November 2, 2026
11,12-Bis(8-isocyanatooctyl)docosane → HCID 178442887, compound
https://huagongshe.com/reaction/1158550
Participants
| Role | Name | HCID | Charge |
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| Reactant | 11,12-Bis(8-isocyanatooctyl)docosane | HCID 59512998 | — |
| Reactant | HCID 178442731 | HCID 178442731 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178442887 | HCID 178442887 | 97.2% |
Reaction Steps
In a 250 mL round-bottomed flask was added 2-amino-6-nonylpyrimidin-4(1H)-one (1.88 g, 7.92 mmol) in Pyridine 50 mL to give a white suspension. The mixture was heated to 50 deg/C. 11,12-bis(8-isocyanatooctyl)docosane (2.327 g, 3.77 mmol) was dissolved in 5-10 mL of pyridine and added all at once to the mixture. The reaction was heated to 75 deg/C. and stirred for 24 h. The pyridine was removed and the residue was taken up in chloroform and the viscous solution was dripped into a rapidly stirring solution (500 mL) of MeOH upon which a white solid formed. The solution was decanted off and the residue was taken up in MeOH (10 ml) and rapidly stirred for 1 h. The product was collected by vacuum filtration dried under vacuum to give 4 g of 1,1′-(9,10-didecyloctadecane-1,18-diyl)bis(3-(6-nonyl-4-oxo-1,4-dihydropyrimidin-2-yl)urea).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07811370B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-19d58ade60d14e67b17ad9b14f067723 |
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| Source note | uspto-grants-2010_10 |
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