HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethylamine hydrobromide → HCID 11469493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 19020440 | HCID 19020440 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11469493 | HCID 11469493 | — |
Reaction Steps
(aca) Method A: 17.4 g of methyl 3-mercapto-thiophene-2-carboxylate were dissolved in 350 ml of toluene under an inert gas atmosphere, whereupon the solution was treated with 20.5 g of 2-aminoethyl bromide hydrobromide and then with 100 ml of 3N sodium methylate solution in methanol. The mixture was stirred at room temperature for 30 minutes and thereafter heated under reflux until the reaction finished. The mixture was evaporated in vacuo, the residue was taken up in 300 ml of water, acidified with 2N hydrochloric acid and the crystals were removed by filtration. By recrystallization from chloroform there was obtained 3,4-dihydro-thieno[2,3-f][1,4]thiazepin-5-(2H)-one as white crystals of m.p. 186°-188°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735940 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-7f3384be380a42fc9f836ec416ac2072 |
| Source note | uspto-grants-1988_04 |