HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxybenzaldehyde → N-(2-Ethylthioethyl)-N-(4-phenoxybenzyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | 2-(Ethylthio)ethylamine hydrochloride | HCID 3016870 | — |
| Product | N-(2-Ethylthioethyl)-N-(4-phenoxybenzyl)amine | HCID 19048210 | 95% |
Reaction Steps
Following the procedure described in Example 68A, 4-phenoxybenzaldehyde (1.98 g, 10 mmol) and 2-(ethylthio)ethylamine hydrogen chloride (1.42 g, 10 mmol) were combined to give the title compound (2.72 g, 95%). 1H NMR (300 MHz, CDCl3), δ 7.33 (m, 4 H), 7.09 (t, 1 H), 6.98 (m, 4 H), 3.78 (s, 2 H), 2.84 (t, 2 H), 2.71 (t, 2 H), 2.54 (q, 2 H), 1.26 (t, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631401 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-2584b6a8aff64f61a562814a6a8d559d |
| Source note | uspto-grants-1997_05 |