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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromobenzene → Diphenylpyrrolidine

HRID 618
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HRID 618 반응식
Brc1ccccc1.c1ccc(C2CCCN2)cc1>C1COCCO1.CC(C)Oc1cccc(OC(C)C)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].[Pd]>c1ccc(C2CCCN2c2ccccc2)cc1
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참가 물질

7

반응물 2

HCID 7961BromobenzeneHCID 2618922-Phenylpyrrolidine

생성물 1

HCID 11218352Diphenylpyrrolidine수율 90.18%

시약·촉매·용매 4

HCID 10796Cesium carbonate시약HCID 9811564Bis(dibenzylideneacetone)palladium촉매
HCID 16217985
2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl
촉매
HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

Caesium carbonate (553 mg, 1.70 mmol) was added to bromobenzene (0.059 mL, 0.57 mmol) and 2-phenylpyrrolidine (100 mg, 0.68 mmol) in 1,4-dioxane (2 mL). The reaction was degassed and Tris(dibenzylideneacetone)?dipalladium(0) (12.96 mg, 0.01 mmol) and dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine (RuPhos) (13.21 mg, 0.03 mmol) were added. The resulting solution was stirred at 100 °C for 16 hours. LCMS showed the formation of the product. The reaction mixture was diluted with EtOAc, and washed with water. The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. NMR confirmed the presence of the product. The crude product was purified by flash silica chromatography, elution gradient 0 to 15% DCM in MeOH. Pure fractions were evaporated to dryness to afford 1,2-diphenylpyrrolidine (114 mg, 90 %) as a brown oil.

출처 및 근거

ORD 기록
ord-9faf2ea031204c63b2d52d8ff6231013
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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