HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 20558013, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | (2-Phenylethyl)thiourea | HCID 735845 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20558013 | HCID 20558013 | 81% |
Reaction Steps
N-phenethylthiourea (225 grams, 1.25 moles) and α-bromoacetophenone (250 grams, 1.25 moles, Aldrich Chem. Co.) in 1500 ml absolute ethanol were heated to reflux temperature for 21/2 hours under nitrogen. After reducing the solvent volume by 10%, the reaction mixture was cooled to room temperature and then to 0° C. in an ice bath. The solids were filtered off, redissolved in 2,500 ml of absolute ethanol and heated to reflux. The solvent volume was reduced to 2000 ml and the reaction mixture cooled to 0° C. This procedure was repeated and after the second recrystallization the solids were collected and dried under vacuum over phosphorous pentoxide, yielding 365 grams (81%) of 2-phenethylamino-4-phenyl-thiazole hydrobromide, m.p. 169°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307106 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-97691aaa5b5b48bda268ee6ef7825ddc |
| Source note | uspto-grants-1981_12 |