HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51189Generated: October 24, 2026
Hydrochloric Acid → Bis(4-n-butylcyclohexylsulfonyl)diazomethane
https://huagongshe.com/en/reaction/51189
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | Bis(4-n-butylcyclohexylsulfonyl)methane | HCID 22737628 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Bis(4-n-butylcyclohexylsulfonyl)diazomethane | HCID 22737649 | 20.6% |
Reaction Steps
In 91 g of dichloromethane were dissolved 10.5 g (0.025 mol) of the bis(4-n-butylcyclohexylsulfonyl)methane prepared above and 7.5 g (0.038 mol) of p-toluenesulfonylazide. The solution was cooled on an ice bath, to which 3.7 ml (0.0025 mol) of diazabicyclo[5.4.0]-7-undecene (DBU) was added dropwise at a temperature below 5° C. The solution was ripened at the temperature for 15 minutes, after which 38 g of water and 10 g of 12N conc. hydrochloric acid were added. The organic layer was separated and washed with 50 g of water. The solvent was distilled off in vacuum, leaving an oily matter. It was purified by silica gel column chromatography (using dichloromethane as a developing solvent), obtaining 2.3 g of the desired bis(4-n-butylcyclohexylsulfonyl)diazomethane. The yield was 20%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713612B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-710f2b20ca6b4f8b8c10f43115d88589 |
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| Source note | uspto-grants-2004_03 |
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