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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27772생성일: 2026년 10월 24일

2-Phenylethanol → Ethyl Acetoacetate

https://huagongshe.com/ko/reaction/27772

반응식

참여 물질

역할이름HCID투입량
반응물2-PhenylethanolHCID 6054—
반응물2,2-DiethoxyethylamineHCID 69524—
반응물3,4-Dimethoxyphenethyl alcoholHCID 81911—
생성물Ethyl AcetoacetateHCID 8868—
생성물1-Methyl-1-isochromanacetic acid ethyl esterHCID 54257169—

반응 단계

In the same manner but replacing 3,4-dimethoxyphenethyl alcohol and aminoacetaldehyde diethyl acetal with equivalent amounts of phenethyl alcohol, Khafagy and Lambooy, cited above, and ethyl acetoacetate, respectively, 1-methyl-1-isochromanacetic acid ethyl ester, νmaxCHCl3 1720 cm-1, nmr (CDCl3) δ1.5, 2.85, is obtained. Likewise, replacement with equivalent amounts of 1-naphthaleneethanol, M. Mousseron and Nguyen-Phuoc-Du. Bull. Soc. Chim. Fr., 91 (1948), and ethyl acetoacetate, gives 1,2-dihydro-4-methyl-4H-naphtho[2,1-c]-pyran-4-acetic acid ethyl ester, νmaxCHCl3 1720 cm-1, nmr (CDCl3) δ1.5. Hydrogen bromide is a preferred acid catalyst for these latter two preparations.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04223151
출처 데이터셋uspto-grants-1980_09
ORD IDord-b6c1b5550c2a4f4f80fcb4ae26c3c1dd
출처 메모uspto-grants-1980_09