홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

3-Phenylphenol → N-tert-Butoxycarbonyl-trans-4-(3-Biphenyloxy)-L-Proline Methyl Ester

HRID 2185493
노트
인쇄 미리보기

반응식

HRID 2185493 반응식
[CH3:1]COC(/N=N/C(OCC)=O)=O.[C:13]([O:17][C:18]([N:20]1[CH2:27][C@H:26]([OH:28])[CH2:25][C@H:21]1[C:22]([OH:24])=[O:23])=[O:19])([CH3:16])([CH3:15])[CH3:14].[C:29]1([C:35]2[CH:36]=[C:37](O)[CH:38]=[CH:39][CH:40]=2)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[CH3:1][O:23][C:22](=[O:24])[C@@H:21]1[CH2:25][C@@H:26]([O:28][C:31]2[CH:30]=[C:29]([C:35]3[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=3)[CH:34]=[CH:33][CH:32]=2)[CH2:27][N:20]1[C:18]([O:17][C:13]([CH3:16])([CH3:14])[CH3:15])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 113813-PhenylphenolHCID 11776TriphenylphosphineHCID 88804(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 5462977Diethyl azodicarboxylate

생성물 1

HCID 21341533N-tert-Butoxycarbonyl-trans-4-(3-Biphenyloxy)-L-Proline Methyl Ester

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

A solution of diethylazodicarboxylate (829 μL) in tetrahydrofuran (10 mL) was added to a cold (−15° C.) stirred solution of N-tert-butoxycarbonyl-trans-4-hydroxy-L-proline (1.23 g), 3-phenylphenol (896 mg), and triphenyl phosphine (1.38 g) in tetrahydrofuran (30 mL) under argon, After stirring at room temperature for 15.5 hr, the solvent was evaporated and coevaporated several times with toluene in vacuo. The residue was diluted with toluene and precipitated solids were removed by filtration, which was washed with toluene. The combined organic layers were evaporated in vacuo and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:10, v/v) to give title compound (837 mg): 1H-NMR (400 MHz, CDCl3) δ 1.36-1.50 (m, 9H), 2.18-2.29 (m, 1H), 2.51-2.64 (m, 1H), 3.68-3.89 (m, 5H), 4.40-4.56 (m, 1H), 4.91-5.01 (m, 1H), 6.79-6.87 (m, 1H), 7.04-7.10 (m, 1H), 7.17-7.24 (m, 1H), 7.29-7.39 (m, 2H), 7.39-7.49 (m, 2H), and 7.49-7.60 (m, 2H).

후처리

  1. customthe solvent was evaporated
  2. additionThe residue was diluted with toluene
  3. customprecipitated solids
  4. customwere removed by filtration, which
  5. washwas washed with toluene
  6. customThe combined organic layers were evaporated in vacuo
  7. customthe residue was purified by silica gel column chromatography (ethyl acetate

출처 및 근거

ORD 기록
ord-f9e90175c4d644828eb67129e09eb16b
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399629B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트