Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
5-[(3-Phenylmethoxy-4-methoxyphenyl)methylene]-2,4-imidazolidinedione → (RS)-5-[[4-Methoxy-3-(phenylmethoxy)phenyl]methyl]-2,4-imidazolidinedione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 5-[(3-Phenylmethoxy-4-methoxyphenyl)methylene]-2,4-imidazolidinedione | HCID 53829032 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Nickel | HCID 935 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (RS)-5-[[4-Methoxy-3-(phenylmethoxy)phenyl]methyl]-2,4-imidazolidinedione | HCID 15296732 | 47% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05525614 |
| 출처 데이터셋 | uspto-grants-1996_06 |
| ORD ID | ord-9ff26a167d074e37b312a7c695ce825e |
| 출처 메모 | uspto-grants-1996_06 |