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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Vinyl-2-norbornene → Bicyclo(2.2.1)hept-2-ene, 5-ethyl-

HRID 1165283
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인쇄 미리보기

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HRID 1165283 반응식
[CH:1]([CH:3]1[CH2:8][CH:7]2[CH2:9][CH:4]1[CH:5]=[CH:6]2)=[CH2:2].C([Al](CC)CC)C>[Cl-].[Cl-].[CH-]1C=CC=C1.[CH-]1C=CC=C1.[Ti+2]>[CH2:1]([CH:3]1[CH2:8][CH:7]2[CH2:9][CH:4]1[CH:5]=[CH:6]2)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 182735-Vinyl-2-norborneneHCID 16682930Triethylaluminum

생성물 1

HCID 85837Bicyclo(2.2.1)hept-2-ene, 5-ethyl-

시약·촉매·용매 1

HCID 124040768Titanocene dichioride촉매

실험 절차

The reaction was carried out in the same way as in Example 1 except that the substrate was changed to 5-vinylbicyclo[2. 2. 1]hept-2-ene, 6 mmol of titanocenedichloride and 60 mmol of triethyl aluminum were charged into the autoclave, and the reaction period was set to five hours, to produce 134.7 g of 5-ethylbicyclo[2. 2. 1]hept-2-ene having the purity of 98.9%. Analyses by proton NMR revealed that only the signal of unsaturated proton of norbornene could be noticed in the vicinity of 5.8 ppm (δ) whereas the signal of unsaturated proton of vinyl in the vicinity of 5.0 ppm (δ) could not be noticed.

후처리

  1. additionwere charged into the autoclave
  2. customthe reaction period

출처 및 근거

ORD 기록
ord-94828a4a448e4323b85812effae1f3cc
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04908420

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