참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| 반응물 | Methyl 2-hydroxy-1-naphthoate | HCID 598533 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 2-(perfluoro-1-butanesulfonyloxy)-1-napthoate | HCID 18353806 | — |
반응 단계
Perfluoro-1-butanesulfonyl fluoride (19 mL, 106 mmol, 1 eq) was added to a solution of methyl 2-hydroxy-1-naphthoate (21.25 g, 105 mmol, 1 eq) and triethylamine (15 mL, 108 mmol, 1 eq) in tetrahydrofuran (150 mL) maintained at an internal temperature about 0° C., under nitrogen. Once the addition was complete, the mixture was allowed to warm to ambient temperature and stirred for 64 hours. Toluene (150 mL) was added causing some precipitation. The solids were removed by filtration through Celiteä and washed with toluene (20 mL). The organic solutions were combined and washed with 2 N HCl (aq) (2×50 mL), water (100 mL), saturated aqueous sodium carbonate solution (100 mL) and brine (100 mL). The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure. Yield 48.79 g, 95%
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06320068B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-0b6ac454dd9f4f31a52a4a5d6e0de927 |
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| 출처 메모 | uspto-grants-2001_11 |
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