Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Hexadecane | HCID 11006 | — |
| Reactant | Methyl Carbamate | HCID 11722 | — |
| Reactant | Heneicosane | HCID 12403 | — |
| Reactant | 1,3-Diisopropenylbenzene | HCID 77353 | — |
| Reactant | HCID 19005703 | HCID 19005703 | — |
| Reactant | HCID 22639212 | HCID 22639212 | — |
| Product | HCID 86739330 | HCID 86739330 | 3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04439616 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-0540be32f00e467db27058557fc23e7c |
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| Source note | uspto-grants-1984_03 |
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