HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 2-Phenyl-5,6,7,8-tetrahydroimidazo[2,1-b][1,3]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 2-Amino-4,5,6,7-tetrahydrobenzothiazole | HCID 18046 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Phenyl-5,6,7,8-tetrahydroimidazo[2,1-b][1,3]benzothiazole | HCID 760886 | — |
Reaction Steps
0.1 m. Quantities of 2-amino-4,5,6,7-tetrahydrobenzothiazole and α-bromoacetophenone in 100 ml. of chloroform are heated at reflux for 2 hours. After cooling, the solid is filtered off and slurred in 1 l. of water containing 40 g. of ammonium acetate. This suspension is heated to boiling over a 2-hour period and allowed to cool. The product is collected, washed with water and dried. The yield of product is 19.8 g. melting at 158°-160° C. and having the formula: ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04419289 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-c976a055a2dd47dbabeb2a294deae55f |
| Source note | uspto-grants-1983_12 |