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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Boron trifluoride etherate → 2,3,4,5-Tetrahydro-1-benzoxepin-4-one

HRID 84617
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인쇄 미리보기

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HRID 84617 반응식
[O:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:11])[CH2:3][CH2:2]1.B(F)(F)F.[CH3:16]COCC.[Si](C=[N+]=[N-])(C)(C)C>C(OCC)C.C(=O)(O)[O-].[Na+]>[O:1]1[CH2:2][CH2:3][C:4](=[O:11])[CH2:16][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:10]1=2
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참가 물질

6

반응물 3

HCID 8000Boron trifluoride etherateHCID 68110ChromanoneHCID 167693Trimethylsilyldiazomethane

생성물 1

HCID 125800312,3,4,5-Tetrahydro-1-benzoxepin-4-one

시약·촉매·용매 2

HCID 3283Diethyl Ether용매3회HCID 516892Sodium Bicarbonate용매

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온도
0 °C

실험 절차

To a solution of 4-chromanone (9.54 g, 64.3 mmol) in diethyl ether at 0° C. was slowly added boron trifluoride diethyl etherate (16.3 ml, 128.6 mmol), followed by the dropwise addition of 2M TMSCHN2 in diethyl ether. The mixture was allowed to stir for 1 hour at 0° C. before diluting with sat. sodium bicarbonate solution and diethyl ether. The organic phase was dried, concentrated, and purified on silica to give 2,3-dihydro-5H-benzo[b]oxepin-4-one.

후처리

  1. customat 0° C.
  2. customThe organic phase was dried
  3. concentrationconcentrated
  4. custompurified on silica

출처 및 근거

ORD 기록
ord-a84fee2c41ce4e6b9f045d6d307b4e1b
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846762B2

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