HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichlone → HCID 178516332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichlone | HCID 8342 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | 4-(4-Chlorophenyl)cyclohexane-1-carboxylic acid | HCID 2735792 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178516332 | HCID 178516332 | 39.8% |
Reaction Steps
A mixture of 2,3-dichloro-1,4-naphthoquinone (57.0 gm), 4-(4-chlorophenyl)-cyclohexane-1-carboxylic acid (60.0 gm) and silver nitrate (42.7 gm) is taken in acetonitrile (600 ml) and then a solution of ammonium persulphate (180.12 gm) in water (780 ml) is added. The mixture is heated to reflux, maintaining good stirring. The mixture was refluxed for 4 hrs. Then cooled in ice for about 1 hr after which it is filtered. The filtrate is kept aside for acetonitrile recovery. The solid is extracted with hot methylene chloride (100 ml×3). The inorganic salt is collected separately for recovery of silver. The organic layer is dried over anhydrous sodium sulphate and concentrated to get light brownish yellow solid (38.5 gm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08283499B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-734842e13652449a97843cf9ccbad59d |
| Source note | uspto-grants-2012_10 |