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

HCID 11299024, 화합물 → 2-Methyl-2-(4-nitrophenyl)propan-1-ol

HRID 238514
노트
인쇄 미리보기

반응식

HRID 238514 반응식
[CH3:1][C:2]([C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=1)([CH3:7])[C:3](OC)=[O:4]>C1COCC1>[CH3:7][C:2]([C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=1)([CH3:1])[CH2:3][OH:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 11299024HCID 11299024, 화합물

생성물 1

HCID 222492792-Methyl-2-(4-nitrophenyl)propan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a stirred solution of methyl 2-methyl-2-(4-nitrophenyl)propionate (5.32 g, 23.8 mmol, Step A) in THF (200 mL) at 0° C. was added a solution of BH3 1M in THF (25.8 mL, 45.8 mmol). The reaction was stirred at RT overnight and quenched with MeOH. THF was evaporated under reduced pressure and the residue was diluted in EtOAc and aqueous 1M HCl was added. The mixture was extracted with EtOAc, the organic layer was dried over MgSO4 and evaporated under reduced pressure. The product was purified by flash chromatography using 40% EtOAc-hexane to give the title compound as a yellow solid.

후처리

  1. customquenched with MeOH
  2. customTHF was evaporated under reduced pressure
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • additionthe residue was diluted in EtOAc
  • additionaqueous 1M HCl was added
  • extractionThe mixture was extracted with EtOAc
  • dry with materialthe organic layer was dried over MgSO4
  • customevaporated under reduced pressure
  • customThe product was purified by flash chromatography
  • 출처 및 근거

    ORD 기록
    ord-81d034130e0a4b889ec7d52cf199769d
    출처 데이터셋
    uspto-grants-2014_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08642624B2

    반응 노트

    불러오는 중…