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HRID 1034350생성일: 2026년 10월 27일

Cycloheptanone → 2-[(Tetrahydropyranyloxy)acetyl]cycloheptanone

https://huagongshe.com/reaction/1034350

반응식

참여 물질

역할이름HCID투입량
반응물CycloheptanoneHCID 10400—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물ethyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetateHCID 10899396—
촉매EthanolHCID 702—
용매MethanolHCID 887—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물2-[(Tetrahydropyranyloxy)acetyl]cycloheptanoneHCID 1496515588.2%

반응 단계

A solution of 2.80 g (25 mmol) of cycloheptanone and 4.71 g (25 mmol) of ethyl (tetrahydropyranyloxy)acetate (Ireland, R. E.; Wipf, P. Tetrahedron Lett., 1989, 30, 919-22) in 20 mL of Et2O was added over the course of 1 h to an ice-cold, stirring mixture of hexane-washed NaH and 0.12 mL (2 mmol, 0.092 g) of absolute EtOH in 10 mL of Et2O under N2. The light brown mixture was allowed to warm to room temperature and was stirred overnight. MeOH (5 mL) was added and the solution was poured onto 200 mL of saturated aqueous NH4Cl. After acidification to pH 2 with 1N aqueous HCl, the mixture was extracted with Et2O. The organic layer was washed with brine, dried over Na2SO4, and concentrated to give 5.61 g of crude 2-[(tetrahydropyranyloxy)acetyl]cycloheptanone as a light brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05315012
출처 데이터셋uspto-grants-1994_05
ORD IDord-0fc612491b464df2ad9d3ebe63f66487
출처 메모uspto-grants-1994_05