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Triphenylphosphine → Diphenyl Ether

HRID 1274479
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HRID 1274479 반응식
C([C:5]1[CH:6]=[C:7](C2OC=C(CCO)N=2)[CH:8]=[C:9](C(C)(C)C)[C:10]=1[OH:11])(C)(C)C.C(NCC[C:31]1[CH:36]=[CH:35][C:34](O)=[CH:33][CH:32]=1)(=O)CC.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O>O1CCCC1>[C:31]1([O:11][C:10]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 5462977Diethyl azodicarboxylateHCID 14717710N-(4-Hydroxyphenethyl)propionamideHCID 135509425HCID 135509425, 화합물

생성물 1

HCID 7583Diphenyl Ether수율 109.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매
2회

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온도
0 °C

실험 절차

To a stirred solution of 2-(3,5-di-t-butyl-4-hydroxyphenyl)-4-(2-hydroxyethyl)oxazole (5.51 g, 17.38 mmole) in tetrahydrofuran (47 ml) was added N-ethyl, N-propionyl tyramine (3.5 g, 15.8 mmole) and triphenylphosphine (4.55 g, 17.38 mmole). After cooling to 0° C., a solution of diethylazodicarboxylate (2.73 ml, 17.38 mmole) in tetrahydrofuran (16 ml) was added dropwise over 10 minutes. The reaction was allowed to warm to room temperature and stir for 22 hours, evaporated, and triturated with methylene chloride (50 ml) and filtered. The filtrate was chromatographed on silica gel twice using methylene chloride-ethyl acetate and hexane-acetone gradients to give the intermediate phenyl ether (2.95 g, 36%):

후처리

  1. temperatureto warm to room temperature
  2. customevaporated
  3. customtriturated with methylene chloride (50 ml)
  4. filtrationfiltered
  5. customThe filtrate was chromatographed on silica gel twice using methylene chloride-ethyl acetate and hexane-acetone gradients

출처 및 근거

ORD 기록
ord-d24e5638a6364f80b55f29fdfd1623a8
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06156748

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