HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene 2,4-Diisocyanate → 1-phenyl-3-n-heptyl-2-S-ethyl isothiourea toluene-2,4-diisocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 1-phenyl-3-n-heptyl-2-S-ethyl isothiourea | HCID 20398505 | — |
| Catalyst | HCID 178513445 | HCID 178513445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-phenyl-3-n-heptyl-2-S-ethyl isothiourea toluene-2,4-diisocyanate | HCID 131712860 | — |
Reaction Steps
The equipment was the same as used in Example 26. 2.78 g (0.01 mole) 1-phenyl-3-n-heptyl-2-S-ethyl isothiourea in 35 ml of tetrahydrofuran were mixed with 0.87 g (0.005 mole) toluene-2,4-diisocyanate. The reaction mixture was then refluxed on a steam bath for 1 hour, then 15 drops of the isothiourea was added, and the reaction mixture was refluxed for an additional hour to react all the isocyanate. The reaction mixture was vacuum evaporated to produce 4.1 g of a viscous, yellow liquid having a nD30 of 1.5737. The product was identified as the title product by IR and NMR spectra analyses. Compound No. 151 in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515813 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-5b2fc316f8214265894e582d4f54d27f |
| Source note | uspto-grants-1985_05 |