HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanol → Cyclohexyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 5-(2,4-Dichlorophenoxy)-2-nitrobenzoyl chloride | HCID 13020298 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyclohexyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate | HCID 21486094 | — |
Reaction Steps
To a stirred solution of cyclohexanol (1.05g., 0.0105 mole) and triethylamine (1.10g., 0.011 mole) in toluene (30 ml.) was added 5-(2',4'-dichlorophenoxy)-2-nitrobenzoyl chloride (3.47g., 0.01 mole). A precipitate of triethylamine hydrochloride occurred immediately. The reaction solution was heated to reflux for one hour, cooled and diluted with diethyl ether (150 ml.). After filtering the triethylamine hydrochloride, the solvent was evaporated to give 4.1g. of a brown oil. A small amount of additional precipitate was filtered off. The ether was again stripped to yield 3.5g. of brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001005 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-c9e2f7d53ff048e39212d9718131f103 |
| Source note | uspto-grants-1977_01 |