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Sodium, 2,4-cyclopentadien-1-yl- → HCID 131724107, 화합물

HRID 988863
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HRID 988863 반응식
[CH-:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[Na+].Br[CH2:8][Si:9]([NH:12][C:13]([CH3:16])([CH3:15])[CH3:14])([CH3:11])[CH3:10]>O1CCCC1>[C:13]([NH:12][Si:9]([CH3:11])([CH3:10])[CH2:8][CH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1)([CH3:16])([CH3:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

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HCID 78681Sodium, 2,4-cyclopentadien-1-yl-HCID 180000441-(bromomethyl)-N-(1,1-dimethylethyl)-1,1-dimethylsilanamine

생성물 1

HCID 131724107HCID 131724107, 화합물수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

32.7 ml of a 2.3 M solution (75 mmol) of sodium cyclopentadienide in tetrahydrofurane was added to a solution of 11.4 g (51 mmol) of 2-bromo-1-tertbutylamino-1,1-dimethylsilaethane. The immediate formation of a pinkish solid was observed, the reaction was continued for 8 hours, then it was concentrated to dryness and it was extracted with hexane, the resulting solution was evaporated in order to give a yellow oil, that corresponds to a mixture of isomers (12.5 g, 60 mmol, yield: 80%). 1H-NMR (CDCl3): 6.5-5.75(m,3H), 2.95(m,2H), 1.90(m,2H), 1.20(s,9H), 0.10(s,6H).

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후처리

  1. concentrationit was concentrated to dryness and it
  2. extractionwas extracted with hexane
  3. customthe resulting solution was evaporated in order
  4. customto give a yellow oil
  5. additionthat corresponds to a mixture of isomers (12.5 g, 60 mmol, yield: 80%)

출처 및 근거

ORD 기록
ord-4637cb414d054494a394713a73ebbfa6
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06635778B1

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