HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127968Generated: October 31, 2026
4-Methoxybenzenesulfonyl chloride → HCID 23471003, compound
https://huagongshe.com/reaction/127968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | HCID 11118784 | HCID 11118784 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23471003 | HCID 23471003 | — |
Reaction Steps
A mixture of 10.35 g. (50 mMol) 4-methoxybenzenesulphonyl chloride and 50 ml. pyridine is added dropwise at 0°-10° C. in the course of 5 minutes to a solution of 11.2 g. (50 mMol) ethyl 4-(2-aminoethyl)-phenoxyacetate in 125 ml. anhydrous pyridine. The reaction mixture is allowed to warm up to ambient temperature and then kept at 60° C. for 45 minutes. Subsequently, the reaction mixture is evaporated to half its volume in a vacuum, then poured into ice-water and acidified with hydrochloric acid. The precipitated viscous mass is dissolved in toluene and the toluene phase successively extracted with dilute hydrochloric acid, an aqueous solution of sodium bicarbonate and water. After drying over anhydrous calcium chloride, the solution is evaporated in a vacuum and the residue triturated with some diethyl ether, crystallization thereby takes place. The product is filtered off with suction and recrystallized from a very small amount of diethyl ether. There are thus obtained 13.0 g. (66% of theory) ethyl 4-[2-(4-methoxybenzenesulphonylamino)-ethyl]-phenoxyacetate; m.p. 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04258058 |
|---|
| Source dataset | uspto-grants-1981_03 |
|---|
| ORD ID | ord-a6f99705f7f24baf96616898dca03d46 |
|---|
| Source note | uspto-grants-1981_03 |
|---|