HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → N-(2-chlorobenzyl)-3-methoxyphenylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3-Methoxyphenyl)acetic acid | HCID 15719 | — |
| Reactant | 2-Chlorobenzylamine | HCID 66648 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2-chlorobenzyl)-3-methoxyphenylacetamide | HCID 2089226 | — |
Reaction Steps
A mixture of 12.5 g of 3-methoxyphenylacetic acid, 21.2 g of 2-chlorobenzylamine, 15.1 g of triethylamine, 19.3 ml of borontrifluoride etherate, and 500 ml of toluene was stirred under reflux for 18 hours using a Dean-Stark moisture trap and allowed to cool. The mixture was extracted with aqueous sodium hydroxide, dilute hydrochloric acid, and water. The remaining organic solution was then evaporated and the residue crystallized from hexane to yield N-(2-chlorobenzyl)-3-methoxyphenylacetamide as a yellow solid, m.p. 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623662 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-e5ff32d385f54149832b99453966ef75 |
| Source note | uspto-grants-1986_11 |