HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | N-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide | HCID 10003333 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)benzamide | HCID 11755784 | — |
Reaction Steps
To a solution of N-[3-(hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide and 3.47 g of methanesulfonyl chloride in 200 ml of tetrahydrofuran is added 3.07 g of triethylamine followed by stirring at ambient temperature for 2 hours. Also added is 21.93 g of lithium bromide followed by stirring at ambient temperature for an additional 3 hours. The mixture is poured into water and extracted with ether. The organic layer is washed with a mixture of brine and saturated sodium bicarbonate then dried. The solvent is removed under vacuum and the residue crystallized from carbon tetrachloride:hexanes to give the desired product as a white solid, m.p. 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225425 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-968b08bd862b4f7db8dbc2772a52cf2a |
| Source note | uspto-grants-1993_07 |