HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzene → Coumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzene | HCID 604152 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Reactant | HCID 15346017 | HCID 15346017 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Coumarin | HCID 323 | — |
Reaction Steps
In this scheme, m-(2-isocyanatoprop-2-yl)-α-methylstyrene (23) and m/p-methylstyrene (24) are polymerised under the action of AIBN as free-radical initiator in toluene at 100° to 110° C. to yield the copolymer (25). The preferred molar proportion x of comonomer (23) is between 0 and 60%. The copolymer (25) obtainable in this manner reacts with 3-(6-hydroxyhexoxycarbonyl)-7-diethylaminocoumarin (26) in the presence of catalytic quantities of dibutyltin dilaurate (DBZD) in refluxing methylene chloride, wherein the copolymer (27) may be obtained with a lateral coumarin luminophore (Et=ethyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891975 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-76085fce72fa4300956c3e69344f09f7 |
| Source note | uspto-grants-1999_04 |