참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,6-Lutidine | HCID 7937 | — |
| 반응물 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 반응물 | 5-Chloro-2-hydroxy-3-nitrobenzoic acid | HCID 412078 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-Chloro-2-trifluoromethanesulfonyloxy-3-nitrobenzoic acid | HCID 23033925 | 95.2% |
반응 단계
2,6-Lutidine (1.83 ml, 15.7 mmol) and trifluoro-methanesulfonic anhydride (3.67 g, 13 mmol) were added dropwise in turn to a solution of methyl ester of 5-chloro-3-nitrosalicylic acid (2.32 g, 10.0 mmol) in methylene chloride (25 ml) with stirring under ice cooling and the mixture was stirred under ice cooling for 0.5 hrs. Methylene chloride (20 ml) and ice water (30 ml) were added to the reaction mixture and the aqueous layer was separated and extracted with methylene chloride. The organic layers were combined, washed with water and dried. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate=10) to give methyl ester of 5-chloro-2-trifluoromethanesulfonyloxy-3-nitrobenzoic acid (3.33 g, 91%) as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07345068B2 |
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| 출처 데이터셋 | uspto-grants-2008_03 |
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| ORD ID | ord-6c43c697bb934391954883510eedae39 |
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| 출처 메모 | uspto-grants-2008_03 |
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