HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexamethylene diisocyanate → HCID 20488677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexamethylene diisocyanate | HCID 13192 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 1-Methylhexahydropyrimidine | HCID 520548 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20488677 | HCID 20488677 | — |
Reaction Steps
168 g of hexamethylenediisocyanate in 150 ml of ethyl acetate are slowly added to a mixture of 224 g of N-methylhexahydropyrimidine and 150 ml of ethyl acetate cooled to temperatures of from 15° to 20° C. Stirring is continued at room temperature after all the diisocyanate has been added until the isocyanate band in the IR spectrum has disappeared (after about 2 hours). The solvent is removed on a thin layer evaporator at 110° C. under a vacuum produced by a water jet pump. The viscous product preferentially consists of the following bis-hexahydropyrimidine derivative: ##STR18##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04404379 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-3c01103a895b463b9f8435b903c4df1e |
| Source note | uspto-grants-1983_09 |