HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12824119, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2,3,5-Trimethyl-6-(5'-carboxypentyl)-1,4-benzoquinone | HCID 12906150 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 12824119 | HCID 12824119 | — |
Reaction Steps
To a well stirred solution of 2,3,5-trimethyl-6-(5'-carboxypentyl)-1,4-benzoquinone (formula I-2 wherein R=H3C, n=4, in the free form) (0.21 part) in ethanol (10 volume parts) was added 3 drops of concentrated sulfuric acid under cooling in ice bath and kept standing for 12 hours. After addition of water, the reaction mixture was extracted with diethyl ether and the diethylether layer was washed with water and dried over anhydrous sodium sulfate. The residue upon removal of the solvent was subjected to chromatography on silica gel and eluted with chloroform to give 2,3,5-trimethyl-6-(5'-ethoxycarbonylpentyl)-1,4-benzoquinone (formula I-2 wherein R=H3C, n=4, in the form of ethyl ester) (0.20 part) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04525361 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-d08b1ec2e60140b6b4b2e5915b615b81 |
| Source note | uspto-grants-1985_06 |