돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759522생성일: 2026년 10월 26일

Phenol → alpha-Hydroxy-beta-Phenoxy-N-(1-Methylethyl)Benzenepropanamide

https://huagongshe.com/reaction/1759522

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물18-Crown-6HCID 28557—
반응물SodiumHCID 5360545—
반응물N-(1-methylethyl)-3-phenyl-2-oxiranecarboxamideHCID 13041334—
용매MethanolHCID 887—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Sodium methanolate methanolHCID 23694274—
생성물alpha-Hydroxy-beta-Phenoxy-N-(1-Methylethyl)BenzenepropanamideHCID 13041337—

반응 단계

Phenol (3.0 g.) was converted into its sodium salt by dissolving in a freshly prepared sodium methoxide-methanol solution (0.7 g. of metallic sodium in 50 ml. of absolute methanol), and subsequent evaporation of the excess methanol under reduced pressure on a rotary evaporator. The solid residue was dissolved in acetonitrile (250 ml.) by stirring with 18-crown-6 (0.9 g.) for 30 minutes at room temperature. N-(1-methylethyl)-3-phenyl-2-oxiranecarboxamide (6.16 g.) was added to the solution, and the resulting mixture was heated under reflux for 6 hours. After cooling to room temperature, it was filtered. The filtrate was evaporated on a rotary evaporator under reduced pressure to give a resinous material. Water (ca. 200 ml.) was added to the residue, and allowed to stand at room temperature. The white precipitate thus separated was collected on a filter and washed with water. The filter residue was dried in air, then recrystallized from ethanol, giving 2.5 g. of product, m.p. 166°-168°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04341718
출처 데이터셋uspto-grants-1982_07
ORD IDord-b94c7c4f3f3345489167438486243d79
출처 메모uspto-grants-1982_07