HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288568Generated: October 31, 2026
p-Toluenesulfonyl azide → HCID 21938930, compound
https://huagongshe.com/reaction/2288568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18699519 | HCID 18699519 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21938930 | HCID 21938930 | — |
Reaction Steps
3.0 g of the cyclohexylsulfonyl-(4-methoxyphenylsulfonyl)methane prepared in (2), was put into a flask, and 100 mL of ethanol was added thereto, followed by stirring. Further, to this solution, 8.0 g of a 5 wt % ethanol solution of sodium hydroxide was added, followed by stirring. This reaction solution was cooled to from -5° C. to -10° C., and 35 mL of pure water was added thereto. Then, 10 mL of the ethanol solution containing 2.0 g of p-toluenesulfonylazide obtained in Reference Example 2, was dropwise added thereto over a period of 5 minutes, and the mixture was stirred for 3 hours and left to stand overnight. Then, the precipitate was collected by filtration to obtain crude crystals. The crude crystals were re-crystallized from ethanol to obtain cyclohexylsulfonyl-(4-methoxyphenylsulfonyl)diazomethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090518 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-cdd7f61155764e3eb4bdc7405af2b10f |
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| Source note | uspto-grants-2000_07 |
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