참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,7-Naphthalenediol | HCID 11397 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 7-Bromo-2-naphthol | HCID 613827 | 43% |
반응 단계
Triphenyl phosphine (89.7 g, 0.342 mol) and acetonitrile (350 mL) were combined in a 1-L flask under N2 atmosphere. The mixture was cooled to 10° C. Bromine (17.6 mL, 0.342 mol) was added dropwise over 10 minutes. The cooling bath was removed and 2,7-dihydroxynaphthalene (50.0 g, 0.312 mol) was added along with 350 mL of CH3CN rinse. The resulting yellow tan mixture was heated at reflux for 3 hours. Acetonitrile was distilled off using a water aspirator over 2 hours resulting in a grayish white solid. The solid was heated to 280° C. over 30 minutes giving a black liquid. The liquid was heated to 310° C. over 20 minutes and the temperature was maintained at 310° C. for an additional 15 minutes until gas evolution ceased. The black mixture was cooled to room temperature. Chromatography yielded 34.5 g of the intermediate title compound as an off-white solid which was 87% pure by HPLC (43% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06844344B2 |
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| 출처 데이터셋 | uspto-grants-2005_01 |
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| ORD ID | ord-573ac339c38149fe8cf5990f4a3211f8 |
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| 출처 메모 | uspto-grants-2005_01 |
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