HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Bromobutyl)phthalimide → N-(4-METHYLSULFANYL-BUTYL)PHTHALIMIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(4-METHYLSULFANYL-BUTYL)PHTHALIMIDE | HCID 10964136 | 91% |
Reaction Steps
A solution of 2-(4-bromo-butyl)-isoindole-1,3-dione (1.00 g, 3.54 mmol) in MeOH (60 mL) was treated with sodium thiomethoxide (0.298 g, 4.25 mmol) and heated to reflux 18 h. The solvent was evaporated in vacuo and the residue partitioned between EtOAc and water. The aqueous layer was further extracted with EtOAc (1×75 mL). The organic layers were dried over MgSO4 and concentrated in vacuo to afford the product 2-(4-methylsulfanyl-butyl)-isoindole-1,3-dione (0.803 g, 91%). 1H NMR (MeOD) 7.844 (m, 4H), 3.704 (t, 2H, J=7.2 Hz), 2.549 (t, 2H, J=7.2 Hz), 2.063 (s, 3H), 1.792 (quint, 2H, J=7.2 Hz), 1.731 (quint, 2H, J=7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138530B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-8fac5d27bd574830a23c8f29c19ef8f1 |
| Source note | uspto-grants-2006_11 |