HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 66702641, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2E)- | HCID 5365867 | — |
| Reactant | 2-Cyano-6-hydroxybenzothiazole | HCID 9881912 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | HCID 66702641 | HCID 66702641 | 120% |
Reaction Steps
To a dry 25-ml round-bottomed flask containing acetone (5 mL), anhydrous potassium carbonate (1.2 g, 8.4 mmole), and geranyl bromide (1.5 mL, 7.3 mmole) was added 6-hydroxy-2-cyanobenzothiazole (1 g, 5.6 mmole). The mixture was refluxed under argon with stirring. Reaction progress was monitored by TLC analysis, developing with 2:1 heptane-ethyl acetate. After 20 h, the potassium carbonate was filtered from the cooled reaction mixture. The solution was concentrated in vacuo to yield 2.1 g of solid. The solid was further purified by flash chromatography using a mixture of 9:1 heptane-ethyl acetate. Appropriate fractions were pooled and evaporated to yield 0.84 g of solid. The structure was confirmed by 1H NMR analysis in DMSO-d6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106052B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2bca2d632ccb4d79af3fbe0931ecdfe9 |
| Source note | uspto-grants-2012_01 |