HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 178473102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178473103 | HCID 178473103 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178473102 | HCID 178473102 | — |
Reaction Steps
To an ice-cold mixture of 4.0 g. (10 mMol) ethyl trans-4-[2-(4-chlorobenzenesulphonylamino)-ethyl]-cyclohexyloxyacetate, 50 ml. methylene chloride and 1.5 g. (15 mMol) triethylamine is added dropwise a mixture of 1.4 g. (10 mMol) benzoyl chloride and 30 ml. methylene chloride. The reaction mixture is maintained for 4 hours at reflux temperature, cooled, filtered and the filtrate washed with dilute hydrochloric acid and water. It is then dried with anhydrous sodium sulphate and evaporated. After purification over silica gel/cyclohexane/diethyl ether (2:1 v/v), there is obtained a yield of 1.7 g. (67% of theory); m.p. 81°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05140038 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-ea8f8b8955a242bd974b6bc77f584649 |
| Source note | uspto-grants-1992_08 |