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t-Butylaminodimethylsilylchloride → HCID 18544229, 화합물

HRID 1268144
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HRID 1268144 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[CH:8]([Li])[CH:7]=[CH:6]2.[CH3:15][C:16]([NH:19][Si:20](Cl)([CH3:22])[CH3:21])([CH3:18])[CH3:17]>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[CH:8]([Si:20]([CH3:22])([CH3:21])[NH:19][C:16]([CH3:18])([CH3:17])[CH3:15])[CH:7]=[CH:6]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11205972t-ButylaminodimethylsilylchlorideHCID 178506818HCID 178506818, 화합물

생성물 1

HCID 18544229HCID 18544229, 화합물수율 94.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

(5,6-Dimethoxy-1H-inden-1-yl)lithium (2.5 g, 13.73 mmol) slurried in 40 mL of THF was added to a solution of N-(tert-butyl)-N-(1-chloro-1,1-dimethylsilyl)amine (3.185 g, 19.22 mmol) in 100 mL of THF over a 25 min period. After stirring for 18 h, the volatile components were removed under reduced pressure. The residue solution was extracted with hexane (40 mL). After filtration the volatile components were removed in under vacuum to give 3.95 g, 94 percent yield of the desired product as a light yellow oil.

후처리

  1. customthe volatile components were removed under reduced pressure
  2. extractionThe residue solution was extracted with hexane (40 mL)
  3. filtrationAfter filtration the volatile components
  4. customwere removed in under vacuum

출처 및 근거

ORD 기록
ord-c544a8ce260e4e6f8c2cec97e1986dee
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06555634B1

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