HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082021Generated: October 29, 2026
4-Toluenesulfonyl chloride → Methyl 2-(4'-p-toluenesulfonyloxymethylphenyl)benzoate
https://huagongshe.com/reaction/1082021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Methyl 4'-(hydroxymethyl)-[1,1'-biphenyl]-2-carboxylate | HCID 15380881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(4'-p-toluenesulfonyloxymethylphenyl)benzoate | HCID 15380883 | 82.4% |
Reaction Steps
10.0 g (41 mmol) of methyl 2-(4'-hydroxymethylphenyl)benzoate was dissolved in tetrahydrofuran (200 ml). 2.0 g (50 mmol) of a 60% sodium hydrode was added thereto under cooling with ice, followed by stirring for one hour. A solution of 8.65 g (45.4 mmol) of p-toluenesulfonyl chloride in tetrahydrofuran (50 ml) was dropwise added thereto. Then, the reaction was effected at room temperature for 2 hours and further reflux by heating was effected for 4 hours. The reaction liquid was cooled and added to a saturated aqueous solution of ammonium chloride. The resulting mixture was extracted with chloroform (200 ml). After the organic phase was washed with water and dried, it was subjected to vacuum concentration. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 13.4 g of the title compound as a was (yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05587504 |
|---|
| Source dataset | uspto-grants-1996_12 |
|---|
| ORD ID | ord-50ef8177ec3d4eabb301782df0b0374f |
|---|
| Source note | uspto-grants-1996_12 |
|---|