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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Borane → 1192474-21-7

HRID 541931
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HRID 541931 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([NH:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH:10]=1)[C:5](O)=[O:6].B>O1CCCC1>[Br:1][C:2]1[CH:10]=[C:9]([NH:11][C:12](=[O:13])[O:14][C:15]([CH3:17])([CH3:16])[CH3:18])[CH:8]=[C:4]([CH2:5][OH:6])[CH:3]=1
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참가 물질

4

반응물 2

HCID 6331BoraneHCID 57962321HCID 57962321, 화합물

생성물 1

HCID 579619961192474-21-7

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
20 °C

실험 절차

A solution of 3-bromo-5-[(tert-butoxycarbonyl)amino]benzoic acid (13.6 g, 43.1 mol) in tetrahydrofuran (44 mL) at 0° C. was treated with 1 M borane in THF (64.6 mL, 64.6 mmol) dropwise and stirred at 20° C. for 1 h. The reaction mixture was concentrated, diluted with ethyl acetate (200 mL), and washed with 1 M HCl (100 mL) and brine (50 mL). The organic layer was separated, dried over anhydrous sodium sulfate, filtered, and evaporated to give the desired product as a colorless oil that was used without further purification. LCMS for C12H16BrNO3Na (M+Na)+: m/z=323.9, 325.9.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with ethyl acetate (200 mL)
  3. washwashed with 1 M HCl (100 mL) and brine (50 mL)
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-93fbf99d6dd94f9fa9d1601b5d3004eb
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871753B2

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