HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylamine → p-Acetoxybenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
Reaction Steps
1.1 ml (5.6 mmol) of dicyclohexylamine are added to 1 g (5.6 mmol) of 4-acetoxybenzoic acid placed in 10 ml of dichloromethane, and the solution is stirred at room temperature for minutes. 400 μl (5.6 mmol) of thionyl chloride are added and this mixture is stirred at room temperature for 2 hours. The reaction medium is diluted with ethyl ether. The precipitate is filtered off and rinsed with ethyl ether. Concentration of the filtrate gives the 4-acetoxybenzoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06927228B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-6b525bc01e5d499b93d1947d82fb90c1 |
| Source note | uspto-grants-2005_08 |