참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butanedione | HCID 650 | — |
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | HCID 178418255 | HCID 178418255 | — |
| 용매 | Tetrahydrofuran toluene | HCID 22635083 | — |
| 생성물 | 3-Hydroxy-3-phenylbutan-2-one | HCID 233220 | 68% |
반응 단계
The process can also be run in mixtures of tetrahydrofuran and toluene, thereby making the process more economical. When 1.1 equivalent of phenylmagnesium bromide (1.9M in 50% THF/PhMe) was added to 2,3-butanedione in 50% THF/PhMe, crude product was isolated in 82.4% yield (Run 10, Table IV) after work-up. Short path vacuum distillation gave 3-hydroxy-3-phenylbutan-2-one in 68% yield. Alternatively, preparation of phenylmagnesium bromide in 38% THF/PhMe, followed by reaction with 2,3-butanedione in 38% THF/PhMe afforded 3-hydroxy-3-phenylbutan-2-one in 66.4% yield (Run 11, Table IV) after work-up and distillation. Similarly phenylmagnessium bromide in 25% THR/PheMe reacted with 2,3-butanedione in 25% THF/PheMe yielded 3-hydroxy-3-phenylbutan-2-one in 56.9% yield after work-up and distillation.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04704475 |
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| 출처 데이터셋 | uspto-grants-1987_11 |
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| ORD ID | ord-cede89cb38c04486bb9c278853a2f81c |
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| 출처 메모 | uspto-grants-1987_11 |
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