참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | p-Toluenesulfonyl azide | HCID 13661 | — |
| 반응물 | Bis(4-n-butylcyclohexylsulfonyl)methane | HCID 22737628 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Bis(4-n-butylcyclohexylsulfonyl)diazomethane | HCID 22737649 | 20.6% |
반응 단계
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%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713612B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-710f2b20ca6b4f8b8c10f43115d88589 |
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| 출처 메모 | uspto-grants-2004_03 |
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