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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424746Generated: October 26, 2026

2-Benzyltoluene → Methoxycarbonylaminohexyl isocyanate

https://huagongshe.com/reaction/1424746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BenzyltolueneHCID 69738—
Reactantmethyl N-[6-(methoxycarbonylamino)hexyl]carbamateHCID 235165—
ReactantDi-n-butyldilauryltinHCID 9809426—
Reactant1-Methylimidazolium 3-propanesulfonateHCID 129739671—
ProductMethoxycarbonylaminohexyl isocyanateHCID 205883985.2%

Reaction Conditions

Temperature240 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927763B2
Source datasetuspto-grants-2015_01
ORD IDord-5efdbf0fbcd7454ba8fe159ee90aae54
Source noteuspto-grants-2015_01