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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494568생성일: 2026년 10월 25일

Cyclohexane, (bromomethyl)- → Methyl 3-cyclohexyl-2-methyl-2-phenylpropanate

https://huagongshe.com/reaction/494568

반응식

참여 물질

역할이름HCID투입량
반응물Cyclohexane, (bromomethyl)-HCID 137636—
반응물Methyl alpha-methylbenzeneacetateHCID 569653—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-cyclohexyl-2-methyl-2-phenylpropanateHCID 6887455184.5%

반응 조건

온도25 °C

반응 단계

A solution of 2-phenyl-propionic acid methyl ester (3.0 g, 18.27 mmol) in tetrahydrofuran (25 mL) at −78° C. was treated dropwise with the lithium hexamethyldisilazide (21.9 mL, 1M in tetrahydrofuran, 21.9 mmol) and stirred for 1 hour. Bromomethyl-cyclohexane (3.09 mL, 21.92 mmol) was added to the reaction and the reaction was allowed to warm to 25° C. and stirred for 18 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the ethyl acetate layers were combined, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane, then 2.5% ethyl acetate in hexane, and 5% ethyl acetate in hexane to give the title compound (4.02 g, 84%). 1H NMR (300 MHz, CDCl3): δ ppm 1.11 (m, 10H) 1.55 (m, 4H) 1.80 (m, 1H) 2.04 (m, 1H) 3.64 (m, 3H) 7.29 (m, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538105B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-ddfb2fe1ac2648dd89fd37fd398aae52
출처 메모uspto-grants-2009_05