HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopropiophenone → HCID 20558016, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopropiophenone | HCID 16452 | — |
| Reactant | 1-(2-Furfuryl)-2-thiourea | HCID 717699 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20558016 | HCID 20558016 | 33.3% |
Reaction Steps
N-furfurylthiourea (0.82 grams, 0.005 moles) and α-bromopropiophenone (1.07 grams, 0.005 moles, Aldrich Chem. Co.) in 11 ml absolute ethanol were heated to reflux temperature under nitrogen for 3 hours. After cooling to room temperature, the solvent was removed under vacuum to give a thick brown oil, which was triturated with five 35 ml portions of refluxing ethyl acetate. The ethyl acetate was reduced in volume to about 25 ml and cooled to room temperature. The precipitated solids were filtered, washed with ethyl acetate and vacuum dried over phosphorous pentoxide, yielding 0.585 grams (33%) of 2-furfurylamino-5-methyl-4-phenyl-thiazole hydrobromide, m.p. 150°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307106 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-2fb5f3923dbe497787edbd608a630467 |
| Source note | uspto-grants-1981_12 |