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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(E)-3-[5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]-2-propen-1-ol → 3-[5-(5-Methylphenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol

HRID 1062
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반응식

HRID 1062 반응식
C[C:2]1[O:6][C:5](C2C=CC=CC=2)=[N:4][C:3]=1[CH2:13][O:14][C:15]1[CH:16]=[CH:17][C:18]2[O:22][C:21](/[CH:23]=[CH:24]/[CH2:25][OH:26])=[CH:20][C:19]=2[CH:27]=1>O1CCCC1.[C].[Pd]>[CH3:20][C:19]1[CH:18]=[CH:17][CH:16]=[C:15]([CH:13]([C:3]2[N:4]=[CH:5][O:6][CH:2]=2)[O:14][C:15]2[CH:16]=[CH:17][C:18]3[O:22][C:21]([CH2:23][CH2:24][CH2:25][OH:26])=[CH:20][C:19]=3[CH:27]=2)[CH:27]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 19694371(E)-3-[5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]-2-propen-1-ol

생성물 1

HCID 196943823-[5-(5-Methylphenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol수율 93%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of (E)-3-[5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]-2-propen-1-ol (2.00 g) in tetrahydrofuran (100 ml), palladium-carbon (5%, 0.30 g) was added, followed by catalytic reduction at room temperature and under an atmospheric pressure of 1 atm. After the catalyst was filtered off, the filtrate was concentrated to yield 3-[5-(5-methylphenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol (yield 93%), which was then recrystallized from acetone-isopropyl ether to yield colorless prisms having a melting point of 101° to 102° C.

후처리

  1. customfollowed by catalytic reduction at room temperature and under an atmospheric pressure of 1 atm
  2. filtrationAfter the catalyst was filtered off
  3. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-a0b0409b86cb49f38ebdef232d24438a
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05723479

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