HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furaldehyde → HCID 11683799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furaldehyde | HCID 10351 | — |
| Reactant | Tetramethylammonium Triacetoxyborohydride (>90%) | HCID 13696215 | — |
| Reactant | HCID 57839257 | HCID 57839257 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11683799 | HCID 11683799 | 75% |
Reaction Steps
To a solution of 3-(3-pyridin-3-yl-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]octane, 3b (0.08 g, 0.134 mmol) in ClCH2CH2Cl (2 mL) was added tetramethyl-ammonium triacetoxyborohydride (0.053 g, 2.01 mmol) and 3-furaldehyde (0.17 mL, 2.0 mmol). The reaction was stirred at rt for 24 h. The reaction was diluted with CH2Cl2 (10 mL) and washed with 1 N NaOH. The organic phase was dried over sodium sulfate, filtered, and concentrated. The crude product was purified via reverse phase chromatography (eluent: CH3CN in H2O containing 0.1% TFA) to yield 0.045 g (75%) of title compound 8-furan-3-ylmethyl-3-(3-pyridin-3-yl-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]-octane, 4b as a TFA salt. MS m/z=449.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589104B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-67837b26cafa40fc84a07e2ea2dd955a |
| Source note | uspto-grants-2009_09 |