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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Bromophenol → 4-Morpholinophenol

HRID 279
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인쇄 미리보기

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HRID 279 반응식
C1COCCN1.Oc1ccc(Br)cc1>CC(C)(C)[O-].CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.Cc1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.[Na+].[Pd].[Pd]>Oc1ccc(N2CCOCC2)cc1
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참가 물질

7

반응물 2

HCID 78084-BromophenolHCID 8083Morpholine

생성물 1

HCID 805104-Morpholinophenol수율 31.25%

시약·촉매·용매 4

HCID 23676156Sodium t-butoxide시약HCID 9811564Bis(dibenzylideneacetone)palladium촉매
HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
촉매
HCID 1140Toluene용매

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온도
100 °C

실험 절차

4-Bromophenol (865 mg, 5 mmol), Tris(dibenzylideneacetone)dipalladium(0) (229 mg, 0.25 mmol), 2-Dicyclohexylphosphino-2',4',6'-tri-iso-propyl-1,1'-biphenyl (238 mg, 0.50 mmol), Morpholine (0.437 mL, 5.00 mmol) and sodium tert-butoxide (1009 mg, 10.50 mmol) were stirred in toluene (5 mL) overnight at 100 °C. The mixture was allowed to cool to ambient temperature. Ethylacetate was added and the mixture was washed with aqueous NaHCO3 (satd.) and water. The organic phase was separated, dried over MgSO4, filtered and the solvent removed by rotary evaporation. The crude product was added to a silica gel column and was eluted with 0-2 % MeOH in DCM. The collected fraction were combined and the solvent was removed by rotary evaporation. 1H NMR in CDCl3 is consistent with desired product MS (m+1) = 180. HPLC Peak RT = 2.55 minutes is product. Purity = 96%.

출처 및 근거

ORD 기록
ord-c3c3446fa521406ab3b5349b3ab1378a
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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