HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 6-benzyl-1-ethyloctahydro-1H-pyrrolo[3,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridine | HCID 11356376 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-benzyl-1-ethyloctahydro-1H-pyrrolo[3,4-b]pyridine | HCID 86729499 | 45.6% |
Reaction Steps
To a solution of 6-benzyloctahydro-1H-pyrrolo[3,4-b]pyridine (5.00 g) in THF was added 80% NaH (3.00 g) at room temperature. The reaction mixture was stirred for 30 min, and 5.3 mL of iodoethane was added dropwise. The reaction mixture was stirred for another 5 h, and then quenched with ice-water. The resulted mixture was extracted with CH2Cl2 (70 mL×5). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was chromatographed with a silica gel column (eluting agent: 30:1 (v/v) DCM/MeOH) to give the title compound as a pale yellow solid (2.58 g, 45.60%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 245.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181277B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-892c5dcd9c524bddb90de900dac7e0ce |
| Source note | uspto-grants-2015_11 |