참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 4-Hydroxybiphenyl | HCID 7103 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | sodium thiosulfite anhydrous | HCID 15847209 | — |
| 반응물 | Sodium Hypochlorite | HCID 23665760 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-Hydroxy-3-iodobiphenyl | HCID 4106140 | — |
반응 단계
Biphenyl-4-ol((5.26 g, 30.9 mmol), sodium iodide (4.635 g, 30.9 mmol), sodium hydroxide (1.276 g, 31.9 mmol) was dissolved in methanol (85 mL) and cooled to 0° C. To the solution was added 12% (w/v) sodium hypochlorite (20 mL) dropwise maintaining the temperature below 4° C. The solution was stirred at this temperature for 1 hour and then 2M sodium thiosulfite (50 mL) wad added and the pH of the solution was adjusted to >pH 7 with 1M HCl. The mixture was filtered and the filtrate was washed with water. The solid was dried in a vacuum oven and then the title product was obtained as crystals after recrystallisation from heptane. Yield 7.08 g, 77%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07612068B2 |
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| 출처 데이터셋 | uspto-grants-2009_11 |
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| ORD ID | ord-015dc7f31fe34963ae9cf14d583f1eee |
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| 출처 메모 | uspto-grants-2009_11 |
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