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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80997생성일: 2026년 10월 25일

Phosphorus oxychloride → (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine

https://huagongshe.com/reaction/80997

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178461168HCID 178461168—
용매1,2-DichloroethaneHCID 11—
생성물(R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidineHCID 5967076961.1%

반응 단계

Neat POCl3 (463.9 ml, 5067 mmol) was added slowly by addition funnel to a 0° C. solution of (R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (152.2 g, 1013 mmol) in DCE (1.2 L). After the addition was complete, the reaction mixture was warmed to room temperature, then heated to reflux and stirred for 70 minutes. The reaction was complete as determined by HPLC. The reaction mixture was cooled to room temperature, and the excess POCl3 was quenched in 4 portions as follows: Reaction mixture transferred to separatory funnel and dripped into a beaker containing ice and saturated NaHCO3 solution cooled in an ice bath. Once the addition of each portion of the reaction mixture was completed, the quenched mixture was stirred for 30 minutes to ensure complete destruction of POCl3 prior to transfer to separatory funnel. The mixture was transferred to the separatory funnel and extracted twice with DCM. The combined extracts were dried (Na2SO4), filtered, and concentrated. The crude was purified on silica gel as follows: silica gel (1 kg) was slurried in 9:1 hexane:ethyl acetate onto a 3 L fritted funnel, silica settled under vacuum, topped with sand. The crude was loaded with a DCM/hexane mixture, and the compound was eluted using 1 L sidearm flasks under vacuum. High Rf byproducts eluted first, then (R)-4-chloro-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine (104.4 g, 61.09% yield) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846683B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0c174ba5ab9549c99011402bdf79b83b
출처 메모uspto-grants-2014_09