HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 59355026, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | DIETHYL BENZYLSUCCINATE | HCID 576172 | — |
| Reactant | HCID 22179298 | HCID 22179298 | — |
| Product | HCID 59355026 | HCID 59355026 | 64% |
Reaction Steps
To a suspension of NaH (2.2 g, 54 mmole) in THF (200 mL) was added diethyl 2-(phenylmethyl)butanedioate (12.5 g, 49.9 mmole). After 30 min at RT, bromomethyl phthalimide was added to the reaction mixture and the contents were stirred for 14 h at RT. The reaction was quenched with H2O (15 mL), diluted with Et2O (300 mL) and layers separated. The organic layer was concentrated under vacuum and the resulting residue recrystallized from EtOH (0°) to give the title compound (13 g, 64%) as a white solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592475B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-8459d796bbf14e5f9ffe24788d4fca24 |
| Source note | uspto-grants-2013_11 |