HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 86745364 | HCID 86745364 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide | HCID 10052253 | — |
Reaction Steps
To a stirred solution of 4.0 g of N-[3-hydroxymethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide in 100 ml of tetrahydrofuran is added 1.19 g of triethylamine followed by 1.34 g of methanesulfonyl chloride. Also added is 7.66 g of lithium bromide and continued stirring for 24 hours. The solvent is removed under vacuum and the residue is partitioned between chloroform and water followed by an additional wash of the organic layer with saturated sodium bicarbonate. The organic layer is dried and filtered through a pad of silica gel. The filtrate is evaporated to a residue which is crystallized from hexane:carbon tetrachloride to give 4.1 g of the desired product as a white powder, 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-e40945d593bf443ebc866c3221ea9d60 |
| Source note | uspto-grants-1993_07 |