HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-N-(2,4-difluorobenzyl)-N-heptylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | N-(2,4-difluorobenzyl)-N-heptylamine | HCID 60663854 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-N-(2,4-difluorobenzyl)-N-heptylacetamide | HCID 69260215 | 80.2% |
Reaction Steps
N-(2,4-difluorobenzyl)-N-heptylamine (2.004 g, 8.304 mmol) was dissolved in DCM (30 ml). It was then cooled in an ice-bath. Triethylamine (1.092 g, 10.796 mmol) was added and then bromacetyl chloride (1.438 g, 9.135 mmol) was dropped in. The mixture was stirred for 2 hours (ice-bath). It was then washed with water (with additional of 1% hydrochloric acid, pH-3), water and brine, and dried (magnesium sulphate) and evaporated. The crude oil product was dissolved in DCM, then loaded onto a column (ISOLUTE®SI 5 g/25 ml) and eluted with more DCM. Oil product 2.412 g was obtained, yield 80%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351858B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-23ad5e5761c045d79bb0dba95df55315 |
| Source note | uspto-grants-2008_04 |