돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220234생성일: 2026년 10월 26일

Triethylamine → rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-one

https://huagongshe.com/reaction/220234

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-HexanoneHCID 11583—
반응물2-Cyclohexen-1-oneHCID 13594—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물Trifluoromethanesulfonic acidHCID 62406—
용매DichloromethaneHCID 6344—
생성물rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-oneHCID 68414355—

반응 단계

Prepared using the method described in Jung, Michael E.; Tetrahedron Letters 2005, 46(30), 5057-5061. To a suspension of 2.8 g of phosphorous pentoxide in 30 mL anh. DCM were added 6.1 mL of 2-hexanone followed by 14.4 mL of 2-cyclohexen-1-one at rt. The suspension was cooled to 0° C. with an ice bath before 13 mL of trifluoromethanesulfonic acid was carefully added. The reaction mixture was warmed to rt and then heated at 40° C. overnight. 27 mL of NEt3 were dropwise added at 0° C., the mixture was stirred at rt for 10 min and then evaporated to dryness. Purification by CC with EtOAc-Hept (25:75) yielded 3.37 g of rac-(1R*,4R*)-6-methyl-5-propyl-bicyclo[2.2.2]oct-5-en-2-one as brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202885B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-f6ef2aac6ebd4c6c9b699b0cedcabd62
출처 메모uspto-grants-2012_06