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Tin tetrachloride → 3-[2-Azido-2-(2-hydroxyethoxy)ethoxy]benzoic acid ethyl ester

HRID 661191
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HRID 661191 반응식
[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH:13]2[O:17][CH2:16][CH2:15][O:14]2)[CH:6]=1)[CH3:2].[N:19]([Si](C)(C)C)=[N+:20]=[N-:21].Cl[Sn](Cl)(Cl)Cl>CO>[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][CH:13]([N:19]=[N+:20]=[N-:21])[O:14][CH2:15][CH2:16][OH:17])[CH:6]=1)[CH3:2]
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참가 물질

5

반응물 3

HCID 24287Tin tetrachlorideHCID 78378AzidotrimethylsilaneHCID 17999177Ethyl 3-((1,3-dioxolan-2-yl)methoxy)benzoate

생성물 1

HCID 597717683-[2-Azido-2-(2-hydroxyethoxy)ethoxy]benzoic acid ethyl ester

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 3-([1,3]-dioxolan-2-ylmethoxy)-benzoic acid ethylester (2.02 g, 8 mmol) and azidotrimethylsilane (1.17 ml, 8.8 mmol) was added SnCl4 (60 μl) at room temperature under nitrogen. After 2 hr, 2% aqueous methanol (10 ml) was added to the reaction mixture and the reaction was stirred at room temperature for 30 minutes. All the solvents were evaporated under reduced pressure. The residue was co-evaporated with ethanol (2×10 ml). The residue was purified by a column chromatography (3×20 cm). The product was eluted with 0 to 1% methanol in DCM. The title compound was obtained as a colourless oil (2.01 g, 85.1%). APCI-MS, m/z 267.90 (M−N2+1).

후처리

  1. customAll the solvents were evaporated under reduced pressure
  2. customThe residue was purified by a column chromatography (3×20 cm)
  3. washThe product was eluted with 0 to 1% methanol in DCM

출처 및 근거

ORD 기록
ord-385816a1286b40f691afd9913414c636
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084590B2

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