HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ammonia dichloromethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-[3-(1-Piperidinyl)propoxy]benzaldehyde | HCID 13795259 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (4-Chloro-phenyl)-[2-(3-piperidin-1-yl-propoxy)-benzyl]-amine | HCID 17962633 | — |
| Product | Ammonia dichloromethane | HCID 22731429 | 1% |
Reaction Steps
A solution of 2-(3-piperidin-1-yl-propoxy)-benzaldehyde (266 mg), 4-chloroaniline (146 mg), and acetic acid (0.07 mL) in DCM (5 mL) was treated with sodium triacetoxyborohydride (400 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (6 mL) and extracted with DCM (3×10 mL). The combined organic phases were dried (sodium sulfate) and evaporated. Chromatography of the residue (1–5% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (246 mg). 1H NMR (400 MHz, CDCl3): 7.28–7.20 (m, 2H), 7.09 (d, J=8.9 Hz, 2H), 6.89 (m, 2H), 6.55 (d, J=8.9 Hz, 2H), 4.30 (d, J=5.6, 2H), 4.18 (m, 1H), 4.05 (t, J=6.3 Hz, 2H), 2.47 (m, 2H), 2.37 (br, 4H), 1.96 (m, 2H), 1.62–1.56 (m, 4H), 1.49–1.42 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186732B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-68e86e996bd247a8b340c25adcb0f288 |
| Source note | uspto-grants-2007_03 |