HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-(Trifluoromethyl)phenyl)propan-2-amine → N-(4-dec-1-ynylbenzyl)-N-{1-methyl-1-[4-(trifluoromethyl)phenyl]ethyl}amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-(Trifluoromethyl)phenyl)propan-2-amine | HCID 22337579 | — |
| Reactant | 4-Dec-1-ynylbenzaldehyde | HCID 57841320 | — |
| Product | N-(4-dec-1-ynylbenzyl)-N-{1-methyl-1-[4-(trifluoromethyl)phenyl]ethyl}amine | HCID 67186483 | 79% |
Reaction Steps
The same procedure as employed in the preparation of Example 226 (step a) but using 4-dec-1-ynylbenzaldehyde and 1-methyl-1-[4-(trifluoromethyl)phenyl]ethylamine gave the title compound as a colorless oil (79%). 1H NMR (CDCl3, 300 MHz) δ 7.74-7.57 (m, 4H), 7.36 (d, J=8.1 Hz, 2H), 7.24 (d, J=8.3 Hz, 2H), 3.48 (s, 2H), 2.41 (t, J=7.2 Hz, 2H), 1.73-1.22 (m, 18H), 0.91 (t, J=7.0 Hz, 3H). M+(LC/MS(ESI)): 430.4. HPLC (Condition A), Rt: 4.69 min (HPLC purity: 99.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592477B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-5990674ef82f4e45abc275a35ea6935f |
| Source note | uspto-grants-2009_09 |