HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → 1-(Bromoacetyl)-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 1,2,3,4-Tetrahydroquinoline | HCID 69460 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(Bromoacetyl)-1,2,3,4-tetrahydroquinoline | HCID 583814 | — |
Reaction Steps
To a stirred solution of 20.2 g. of bromoacetyl bromide in 150 ml. of benzene is added dropwise over 30 minutes, 26.6 g. of 1,2,3,4-tetrahydroquinoline dissolved in 35 ml. of benzene. The reaction mixture is then stirred at room temperature for 18 hours, after which time the precipitate is filtered off. The resultant filtrate is washed successively with 1N HCL solution and with a saturated sodium chloride solution, dried, and the solvent removed under reduced pressure to yield 1-(bromoacetyl)-1,2,3,4-tetrahydroquinoline, b.p. 70°-80° C. (at 0.1 mm. Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04015005 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-ce6c420f2dd44392ad412c7d98e22342 |
| Source note | uspto-grants-1977_03 |