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Diethylamine → N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)amine

HRID 595101
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HRID 595101 반응식
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].Br[CH2:7]/[CH:8]=[CH:9]\[Sn:10]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:11][CH2:12][CH2:13][CH3:14]>C1COCC1>[CH2:1]([N:3]([CH2:4][CH3:5])[CH2:7]/[CH:8]=[CH:9]\[Sn:10]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:11][CH2:12][CH2:13][CH3:14])[CH3:2]
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참가 물질

4

반응물 2

HCID 8021DiethylamineHCID 10949620[(Z)-3-bromoprop-1-enyl]-tributylstannane2회

생성물 1

HCID 86684726N,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)amine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Diethylamine (19 mL) was added to a solution of ((Z)-3-bromoprop-1-enyl)-tributyl-stannane (Intermediate 4, 7.52 g) in THF (60 mL) and the mixture was stirred for 3 hours. The reaction mixture was evaporated to dryness and the residue was purified by chromatography on a silica column which had been pre-washed with 20% triethylamine in acetonitrile. The column was eluted with a mixture of ethyl acetate and pentane with a gradient of 0-10% to give N,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (4.75 g) as an orange oil.

후처리

  1. customThe reaction mixture was evaporated to dryness
  2. customthe residue was purified by chromatography on a silica column which
  3. washhad been pre-washed with 20% triethylamine in acetonitrile
  4. washThe column was eluted with a mixture of ethyl acetate and pentane with a gradient of 0-10%

출처 및 근거

ORD 기록
ord-c4fd2939367044a89484a0d7986af77c
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242997B2

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