HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 6-Benzyl-1-methyloctahydropyrrolo[3,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridine | HCID 11356376 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 6-Benzyl-1-methyloctahydropyrrolo[3,4-b]pyridine | HCID 15070008 | 45% |
Reaction Steps
A solution of 6-benzyloctahydro-1H-pyrrolo[3,4-b]pyridine (2.00 g) and 37% HCHO (6.0 mL) in HCO2H was heated to 90° C. and stirred for 4 h. The reaction mixture was cooled to rt and poured into ice-water. The mixture was adjusted to pH 10 with 2M NaOH aqueous solution and extracted with CH2Cl2 (70 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as pale yellow oil (0.95 g, 45.00%), HPLC: 85.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 231.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181277B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-28438f15f21d400c9a2537d9d40c9146 |
| Source note | uspto-grants-2015_11 |