HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → 2-(3-(phenylthio)propyl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-(Phenylsulfanyl)propan-1-ol | HCID 5155841 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-(phenylthio)propyl)-1H-isoindole-1,3(2H)-dione | HCID 265185 | 85% |
Reaction Steps
Diethyl azodicarboxylate (14 ml, 89 mmol) was added over 3 minutes to a stirred solution of 3-phenylthiopropanol (14.91 g, 89 mmol), triphenylphosphine (23.25 g, 89 mmol) and phthalimide (13.05 g, 89 mmol) in tetrahydrofuran (350 ml) at room temperature. After 15 hours, the mixture was concentrated in vacuo. Flash chromatography of the residue, eluting with 1:1 ether/hexane, gave the title compound as a white solid (22.5 g 85%). NMR (200 MHz, CDCl3): δ 2.0 (q, 2H), 2.95 (t, 2H), 3.85 (t, 2H), 7.25 (m, 5H), 7.8 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933369 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-00f34f00c22b493a8d26f7a1f2502a40 |
| Source note | uspto-grants-1990_06 |