HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Benzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | HCID 68314438 | HCID 68314438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amine | HCID 68314456 | — |
Reaction Steps
To a solution of 2-[4-(4-fluorophenyl)oxan-4-yl]ethan-1-amine (250 mg, 1.12 mmol) in anhydrous CH2Cl2 (5 ml) and NA2SO4 (159 mg, 1.12 mmol) at rt was added benzaldehyde (0.17 ml, 1.68 mmol). The reaction was stirred overnight. The reaction mixture was filtered and concentrated. The residue was dissolved in 5 ml MeOH at 0° C. and NaBH4 added in one portion (51 mg, 1.34 mmol). The reaction was stirred at 0° C. for 1 h. The solution was then quenched with H2O (10 ml), extracted with CH2Cl2 (3×20 ml), washed with brine (10 ml) and dried over NA2SO4. Purified by normal phase SiO2 chromatography (0 to 10% MeOH/CH2Cl2) to give benzyl({2-[4-(4-fluorophenyl) oxan-4-yl]ethyl})amine as a colorless oil (200 mg, 60%, m/z: 314.2 [M+H]+ observed).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835488B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-badf241c33f44666bbd223fe295d6b54 |
| Source note | uspto-grants-2014_09 |