HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20277060, compound → HCID 20277073, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20277060 | HCID 20277060 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20277073 | HCID 20277073 | — |
Reaction Steps
A solution of 2,3,5-trimethyl-6-(6'-hydroxy-1'-oxohexyl)-hydroquinone (formula III-1 wherein R=H3C, X=Y=OH, n=4, in the free form) (0.1 part) in diethyl ether (10 volume parts) was stirred with 3% aqueous ferric chloride solution at room temperature for 2 hours. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer and diethyl ether extract were washed with water, dried over anhydrous sodium sulfate, and evaporated in vacuo to dryness. The residue was subjected to chromatography on silica gel and eluted with diethyl ether to give 2,3,5-trimethyl-6-(6'-hydroxy-1'-oxohexyl)-1,4-benzoquinone (formula IV-1 wherein R=H3C, n=4, in the free form) (0.088 part) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04271083 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-4930128e978e4337abac7a8e157f93e8 |
| Source note | uspto-grants-1981_06 |