참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| 반응물 | 2-Aminobenzonitrile | HCID 72913 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-Amino-4'-fluorobenzophenone | HCID 9837287 | — |
반응 단계
A solution of 4-bromofluorobenzene (1 eq.) in THF was cooled to −78° C. under nitrogen and treated with tert-butyllithium (2.05 eq., 1.6 M solution in pentane) at a rate of 40 ml/h. The internal temperature did not rise above −74° C. The orange solution was stirred at −78° C. for 30 minutes prior to the addition of anthranilonitrile (0.6 eq.) as a solution in THF. The reaction was warmed to 0° C. and stirred for 2 hours. 3N HCl was added to the mixture and stirring continued for 30 minutes. The reaction was diluted with ethyl acetate and the layers were separated. The aqueous layer was back-extracted thrice with ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified via HPLC eluting with 93:7 hexanes/ethyl acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390801B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-b8d76b83df764b17b38850a4e0b8b51e |
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| 출처 메모 | uspto-grants-2008_06 |
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