HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → (p-bromobenzyl)diethyl amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (p-bromobenzyl)diethyl amine | HCID 10999178 | 88% |
Reaction Steps
A mixture of 4-bromobenzyl bromide (1.0 g, 4.0 mmol), triethylamine (0.84 mL, 6.0 mmol) and diethylamine (0.84 mL, 8.0 mmol) in THF (20 mL) was stirred at ambient temperature for 16 h. The solvent was evaporated and the resultant residue diluted with saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate (2×50 mL). The combined organic layer was dried over sodium sulfate, filtered and evaporated to afford the title compound (0.85 g, 88%). 1H NMR (CDCl3, 300 MHz): 7.45-7.38 (m, 2H), 7.27-7.18 (m, 2H), 3.50 (s, 2H), 2.50 (q, J=7.1 Hz, 4H), 1.03 (t, J=7.1 Hz, 6H). LCMS (Method G): RT=1.98 min, M−H+=242.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501765B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-0044aa76cebc47ff9f92e59c7ed81b6e |
| Source note | uspto-grants-2013_08 |