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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403574생성일: 2026년 10월 24일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 6-allyl-3-((S)-3,3-dimethylbutan-2-yl)-6-(4-fluorophenyl)-1,3-oxazinan-2-one

https://huagongshe.com/ko/reaction/403574

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물(S)-3-isocyanato-2,2-dimethyl-butaneHCID 12169316—
반응물1-Chloro-3-(4-fluorophenyl)hex-5-en-3-olHCID 53472938—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물6-allyl-3-((S)-3,3-dimethylbutan-2-yl)-6-(4-fluorophenyl)-1,3-oxazinan-2-oneHCID 5848525711.4%

반응 단계

A mixture of 1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol (500 mg, 2.19 mmol), (S)-3-isocyanato-2,2-dimethyl-butane (845 mg, 5.58 mmol), and DBU (681 mg, 5.9 mmol) in THF (10 mL) was heated to reflux for 25 h. The mixture was diluted with EtOAc and washed with 1 N aq HCl. The aqueous phase was extracted with EtOAc (3×). The combined organic phase was dried over Na2SO4. After the solvents were evaporated, the crude product was purified by column to give 6-allyl-3-((2S)-3,3-dimethylbutan-2-yl)-6-(4-fluorophenyl)-1,3-oxazinan-2-one (80 mg, crude).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748444B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6e39b42537b94cbf88c34937e4d880c9
출처 메모uspto-grants-2014_06