HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → HCID 4102537, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 4-Bromophthalimide | HCID 236018 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 4102537 | HCID 4102537 | 88.9% |
Reaction Steps
To a suspension of 5-bromo-1H-isoindole-1,3(2H)-dione (ABCR, 5.0 g) and triphenylphosphine (8.70 g) in tetrahydrofuran (THF) (100 mL) under nitrogen at room temperature was added di-t-butyl azodicarboxylate (7.64 g). The suspension was cooled in an ice/water bath and to this was added iso-propanol (2.032 mL). The reaction mixture was allowed to warm to room temperature to give a pale yellow solution. After 60 minutes, the solvent was removed in vacuo and the residue was dissolved in DCM (30 mL). This was applied to a 750 g silica cartridge and eluted with a gradient of 0-40% ethyl acetate in cyclohexane over 8CV. The required fractions were combined and evaporated in vacuo to give the title compound (5.27 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354539B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-fb5cc92bb23b4baf833f0f06c7dff1d9 |
| Source note | uspto-grants-2013_01 |