HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-methylbutan-2-one → HCID 20084355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-methylbutan-2-one | HCID 10899037 | — |
| Reactant | HCID 20084363 | HCID 20084363 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20084355 | HCID 20084355 | — |
Reaction Steps
A solution composed of 2.0 g of (E)-3-(2-chloro-5-nitrophenyl)-2-propenethioamide, 3.0 g of 1-bromo-3-methyl-2-butanone and 25 ml of ethyl alcohol was warmed to gentle reflux for 5 hr. The volatiles were then removed in vacuo and the residual materials separated by chromatography over 100 g of alumnia using methylene chloride as the eluant to yield (E)-2-[2-(2-chloro-5-nitrophenyl)ethenyl]-4-(1-methylethyl)thiazole as a yellow solid; m.p. 86°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273986 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-cb3f952d38004e14b263721e60d4e670 |
| Source note | uspto-grants-1993_12 |