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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260075생성일: 2026년 10월 25일

5-[(3-Phenylmethoxy-4-methoxyphenyl)methylene]-2,4-imidazolidinedione → (RS)-5-[[4-Methoxy-3-(phenylmethoxy)phenyl]methyl]-2,4-imidazolidinedione

https://huagongshe.com/reaction/260075

반응식

참여 물질

역할이름HCID투입량
반응물5-[(3-Phenylmethoxy-4-methoxyphenyl)methylene]-2,4-imidazolidinedioneHCID 53829032—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물(RS)-5-[[4-Methoxy-3-(phenylmethoxy)phenyl]methyl]-2,4-imidazolidinedioneHCID 1529673247%

반응 단계

A solution of 16.20 g (0.05 mole) of the benzylidene hydantoin from Example 4 in 100 mL of methanol and 25.0 g (0,055 mole) of 20% tetramethylammonium hydroxide-in-methanol is reduced with hydrogen and Raney nickel catalyst. After the theoretical uptake of hydrogen the mixture is filtered and acetic acid (ca 5 mL) and then water is added until just turbid. The first crop of solid is filtered. This is starting material. An additional 2 L of water is added to precipitate the product as crop 2; wt 7.60 g (47% yield). Recrystallization from methanol gives pure product; mp 155°-157° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05525614
출처 데이터셋uspto-grants-1996_06
ORD IDord-9ff26a167d074e37b312a7c695ce825e
출처 메모uspto-grants-1996_06