참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | 1-Naphthol | HCID 7005 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Bromo-1-naphthol | HCID 150849 | — |
| 반응물 | N-bromo-t-butylamine | HCID 11789384 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-Bromo-1-methoxynaphthalene | HCID 12612830 | — |
반응 단계
1-naphthol was converted into 2-bromo-1-naphthol by reaction with a slurry of N-bromo-t-butylamine at -78° C. according to the procedure described in Pearson, Wysong, Breder, J. Org. Chem., 32, 2358 (1967). To a solution of 1 mole (crude) of the bromonaphthol in 750 mL of acetone was added 175 g of potassium carbonate. Over a 2-hour period, 95 mL of dimethylsulfate was added dropwise to the mechanically stirred reaction mixture. The resulting slurry was stirred at 25° C. overnight. The solids were filtered and the solution was stripped to yield a dark brown oil. Initial purification was accomplished by vacuum distillation (80-120° C., 0.2 Torr) followed by further purification by HPLC with hexane to yield 145 g of 2-bromo-1-methoxynaphthalene as a pale yellow oil. NMR confirmed the structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06103912 |
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| 출처 데이터셋 | uspto-grants-2000_08 |
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| ORD ID | ord-8892f8ab1d414635ac31f0c310d243eb |
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| 출처 메모 | uspto-grants-2000_08 |
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