돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 246882생성일: 2026년 10월 26일

Butanedione → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/246882

반응식

참여 물질

역할이름HCID투입량
반응물ButanedioneHCID 650—
반응물TolueneHCID 1140—
반응물TetrahydrofuranHCID 8028—
반응물HCID 178418255HCID 178418255—
용매Tetrahydrofuran tolueneHCID 22635083—
생성물3-Hydroxy-3-phenylbutan-2-oneHCID 23322068%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04704475
출처 데이터셋uspto-grants-1987_11
ORD IDord-cede89cb38c04486bb9c278853a2f81c
출처 메모uspto-grants-1987_11