홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 1923445
노트
인쇄 미리보기

반응식

HRID 1923445 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]
참가 물질실험 절차후처리출처 및 근거반응 노트

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 ethyl ester (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 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 column chromatography (3×20 cm)
  3. washThe product was eluted with 0 to 1% methanol in DCM

출처 및 근거

ORD 기록
ord-9ae0b17edb614f39b01cce98bf776822
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178360B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트