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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904106Generated: November 2, 2026

Sulfuric Acid → HCID 86739330, compound

https://huagongshe.com/reaction/1904106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CarbonateHCID 10340—
ReactantHexadecaneHCID 11006—
ReactantMethyl CarbamateHCID 11722—
ReactantHeneicosaneHCID 12403—
Reactant1,3-DiisopropenylbenzeneHCID 77353—
ReactantHCID 19005703HCID 19005703—
ReactantHCID 22639212HCID 22639212—
ProductHCID 86739330HCID 867393303%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a flask containing 59.30 g (789.92 mmoles) of molten methyl carbamate (85° C. oil bath) was added 260 mg (2.6 mmole) of conc.sulfuric acid. The temperature of the oil bath was then lowered to 60° C., and 14.79 g (93.61 mmoles) of m-DIPEB added dropwise to the reaction mixture. The reaction mixture was stirred 60° C. for 4.5 hours, and 500 mg of anhydrous sodium carbonate added to neutralize the acid catalyst. The mixture was stirred at 60° C. for another 30 minutes and then distilled under the vacuum 95°/30 mm Hg) to recover unreacted methyl carbamate (44.05 g; >90% recovery). GLC analyses of the white residue showed that m-TMXDU and m-TMU were formed in 65% and 24% yields, respectively. The solid was then mixed with 50 g of hexadecane and 1.66 g of heneicosane (GLC internal standard), and the mixture cracked at 265° C. for 4 hours. GLC analyses indicated that α,α,α',α'-tetramethyl meta-xylene diisocyanate (m-TMXDI) (45%), meta-isopropenyldimethylbenzene isocyanate (m-TMI) (10%) and α,α,α',α'-tetramethyl-meta-xylene monourethane monoisocyanate (m-TMXUI) (3%) were formed based on the m-DIPEB.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04439616
Source datasetuspto-grants-1984_03
ORD IDord-0540be32f00e467db27058557fc23e7c
Source noteuspto-grants-1984_03