참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Phosphorus tribromide | HCID 24614 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Bromocresol | HCID 41663 | — |
반응 단계
To a stirred solution of PBr3 (1.38 g, 5.0 mmol) in dry THF (2 ml) at −5° C. was added a solution of dry pyridine (0.201 ml) in dry THF (0.4 ml). A solution of 4-Hydroxybenzyl alcohol (1.89 g, 15.2 mmol) in dry THF (23 ml) was added drop wise to the reaction mixture. The reaction mixture was allowed to stand at room temperature for 18 hours, then diluted with THF and filtered through celite pad. The filtrate was evaporated, the resulting semisolid was redissolved in dry toluene (16 ml). The solution was maintained at −20° C. for 2 hours, and then filtered through celite pad to provide the title compound as a light yellow solution which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06946491B2 |
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| 출처 데이터셋 | uspto-grants-2005_09 |
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| ORD ID | ord-300b985d8cc34e6da9f45d5063db6052 |
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| 출처 메모 | uspto-grants-2005_09 |
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