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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639422Generated: October 31, 2026

Methanesulfonic Acid → Toluene 2,4-Diisocyanate

https://huagongshe.com/reaction/1639422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 131716201HCID 131716201—
SolventO-XyleneHCID 7237—
ProductToluene 2,4-DiisocyanateHCID 1144398%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 12.7 g 2,4-toluene bis (diethylurea) in 248 g o-xylene was charged to a 500 ml fluted flask equipped with a bottom take-off, a mechanical stirrer using a 1.5 inch "Teflon" crescent-shaped paddle, a condenser, and a thermocouple to monitor reaction temperature. The mixture was heated to 120° C. and then 8.75 g methane sulfonic acid was added in one portion. The mixture was stirred for 15 min at 120° C. and then the phases were allowed to settle at 50° C. The bottom salt phase was drawn off through the bottom take-off. Analysis of the xylene phase by HPLC and infrared analysis showed 100% conversion of the toluene bis (diethylurea) with a 98% yield of toluene diisocyanate. The xylene phase was then transferred to a round bottom flask equipped with a 12" Vigreux column and a distillation head for vacuum distillation. Octadecane, 65 g, was added to the flask and then the xylene was distilled overhead at 40 mm Hg. TDI was then distilled over 10 mm Hg. A heart cut of TDI containing 6.1 g TDI was obtained for an isolated yield of 88% for toluene diisocyanate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883908
Source datasetuspto-grants-1989_11
ORD IDord-9d213ee9d30f44bf87c4b03268a905ce
Source noteuspto-grants-1989_11