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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactantp-Toluenesulfonyl azideHCID 13661—
ReactantBis(4-n-butylcyclohexylsulfonyl)methaneHCID 22737628—
SolventDichloromethaneHCID 6344—
ProductBis(4-n-butylcyclohexylsulfonyl)diazomethaneHCID 2273764920.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713612B2
Source datasetuspto-grants-2004_03
ORD IDord-710f2b20ca6b4f8b8c10f43115d88589
Source noteuspto-grants-2004_03