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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479246생성일: 2026년 10월 26일

Allyl bromide → [Rac]-3-(3-allyl-4-hydroxy-naphthalen-1-yl)-2-ethoxy-propionic acid ethyl ester

https://huagongshe.com/reaction/479246

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
반응물[Rac]-2-ethoxy-3-(4-hydroxy-naphthalen-1-yl)-propionic acid ethyl esterHCID 68616503—
반응물[Rac]-3-(4-allyloxy-naphthalen-1-yl)-2-ethoxy-propionic acid ethyl esterHCID 69557260—
용매AcetoneHCID 180—
생성물[Rac]-3-(3-allyl-4-hydroxy-naphthalen-1-yl)-2-ethoxy-propionic acid ethyl esterHCID 6955810994%

반응 조건

온도160 °C

반응 단계

0.87 g (2.65 mmol) [rac]-3-(4-allyloxy-naphthalen-1-yl)-2-ethoxy-propionic acid ethyl ester [prepared from [rac]-2-ethoxy-3-(4-hydroxy-naphthalen-1-yl)-propionic acid ethyl ester (example 150 a] and allylbromide, potassium carbonate in acetone at 60° C.] was stirred for 2 hours at 160° C. without any solvent. The dark residue was purified by flash chromatography (silica gel, hexane/AcOEt=4:1) to yield 0.82 g (94%) of [rac]-3-(3-allyl-4-hydroxy-naphthalen-1-yl)-2-ethoxy-propionic acid ethyl ester as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642389B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-5fdaa05bc7494ac5a2f0226384b2d8b5
출처 메모uspto-grants-2003_11