HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Phenyl 4-chloro-3-nitrobenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Phenyl 4-chloro-3-nitrobenzenesulfonate | HCID 266121 | 86.4% |
Reaction Steps
3-Nitro-4-Chloro-benzene-sulfonic acid-phenylester was obtained by mixing 51 g of 3-nitro-4-chloro-benzene-sulfonic acid-chloride with 18.8 g of phenol in 120 ml of acetone, and by adding 28 ml of triethylamine dropwise, while cooling, at a temperature not exceeding 10° C. The mixture was continued to be stirred for several hours at room temperature, and then water was added, in which process an oil was separated which was extracted with ether. After recrystallization of the residue from methanol, 54 g of 3-nitro-4-chloro-benzene-sulfonic acid-phenylester were obtained, which had a melting point of 71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04069325 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-68f9f87caa824dce93a2d5dd5a4266ed |
| Source note | uspto-grants-1978_01 |