HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424746Generated: October 26, 2026
2-Benzyltoluene → Methoxycarbonylaminohexyl isocyanate
https://huagongshe.com/reaction/1424746
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Benzyltoluene | HCID 69738 | — |
| Reactant | methyl N-[6-(methoxycarbonylamino)hexyl]carbamate | HCID 235165 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Reactant | 1-Methylimidazolium 3-propanesulfonate | HCID 129739671 | — |
| Product | Methoxycarbonylaminohexyl isocyanate | HCID 20588398 | 5.2% |
Reaction Steps
500 mL 3-necked flask equipped with a reflux apparatus, cooler, thermometer and sampling device was charged with 1,6-bis(methoxycarbonylamino)hexane (HDC, 50 g), benzyltoluene (250 g), di-n-butyltin dilaurate (0.05 g), and 1-methylimidazolium-3-propanesulfonate (0.1 g) as a zwitterionic compound, which were heated to 240° C. under 20 mmHg pressure. The reaction time was 2 hours, and the temperature of the reflux and cooling condenser was kept at 60° C. or more to prevent the reverse reaction. The resulting 1,6-diisocyanatohexane (HDI) and methanol were separately collected into a flask and dry ice-acetone trap. After the completion of the reaction, the product collected in the flask was analyzed with gas chromatography, which showed 94.1% yield of HDI, 5.2% yield of 1-isocyanato-6-methoxycarbonylaminohexane (HMI), and only 1.3 g of high-boiling polymer precipitates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927763B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-5efdbf0fbcd7454ba8fe159ee90aae54 |
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| Source note | uspto-grants-2015_01 |
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