Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 23138-53-6 | HCID 280454 | — |
| Reactant | Isoindoline | HCID 422478 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68748359 | HCID 68748359 | — |
Reaction Steps
Isoindoline (1.693 ml, 14.47 mmol) was dissolved in tetrahydrofuran (20 ml) and cooled to 0° C.; and methyl 4-isocyanatobenzoate (2.18 g, 12.06 mmol) was added by syringe and the resulting mixture was warmed to ambient temperature, and then stirred overnight. The solution was concentrated to a slurry, diluted with ether, and filtered to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09302989B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8c9f8c65e6764971b49cc7a235da57bc |
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| Source note | uspto-grants-2016_04 |
|---|