HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913231Generated: October 31, 2026
4-Toluenesulfonyl chloride → HCID 67410578, compound
https://huagongshe.com/reaction/913231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11815996 | HCID 11815996 | — |
| Reactant | 1-phenyltetrazole-5-thiol | HCID 178527986 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67410578 | HCID 67410578 | 99.9% |
Reaction Steps
To a solution of (1S)-1-(1-ethylcyclobutyl)-propane-1,3-diol (8.90 g) in toluene (110 mL) were added tetrabutylammonium chloride (1.56 g) and a 2N aqueous sodium hydroxide solution (170 mL). At an inner temperature about 25° C., tosyl chloride (11.3 g) was added to the reaction solution, which was stirred at 25° C. for 1 hour. 1-Phenyl-1H-tetrazol-5-thiol (11.0 g) was added to the reaction solution, which was stirred at 60° C. for 1 hour. After cooling, water was added to the reaction solution, which was separated. The water layer was extracted with t-butyl methyl ether. The mixed organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and concentrated to give the title compound (17.9 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08026273B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-e0c2c30b59e34ba8bc58f444002312fa |
|---|
| Source note | uspto-grants-2011_09 |
|---|