HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839264Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 20324082, compound
https://huagongshe.com/reaction/839264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Carbamic acid, hydroxy-, butyl ester | HCID 164691 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20324082 | HCID 20324082 | — |
Reaction Steps
26.6 Parts of butyl N-hydroxycarbamate and 38.1 parts of p-toluenesulphonylchloride are stirred in 100 parts of dioxan maintained at 0° to 5° C. 20.4 Parts of triethylamine are added during 1 hour keeping the pH at 3 to 6. The mixture is then stirred for 18 hours at 25° C and added to 500 parts of water. The oily precipitate is taken up into 200 parts toluene, and the solution is dried, filtered and evaporated to constant weight at 40° C under reduced pressure to give 52 parts of butyl N-p-toluenesulphonyloxycarbamate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04094863 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-e67c88ef87754f8e9b14457a593cc032 |
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| Source note | uspto-grants-1978_06 |
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