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

Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate → (2-Bromo-4-methylthiazol-5-yl)methanol

HRID 1406301
노트
인쇄 미리보기

반응식

HRID 1406301 반응식
[Br:1][C:2]1[S:3][C:4]([C:8](OCC)=[O:9])=[C:5]([CH3:7])[N:6]=1.[BH4-].[Na+]>CCO.O>[Br:1][C:2]1[S:3][C:4]([CH2:8][OH:9])=[C:5]([CH3:7])[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2824057Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylateHCID 4311764Sodium borohydride

생성물 1

HCID 59295463(2-Bromo-4-methylthiazol-5-yl)methanol수율 65.2%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

To a solution of ethyl 2-bromo-4-methylthiazole-5-carboxylate (7 g, 28 mmol) in EtOH (120 mL) and H2O (20 mL) was added portion-wise NaBH4 (3.2 g, 84 mmol). After the addition, the mixture was stirred at room temperature overnight. TLC (petroleum ether/EtOAc=5:1) showed the reaction was complete. The reaction mixture was carefully concentrated in vacuum. The residue was separated between EtOAc (50 mL) and H2O (50 mL). The inorganic layer was extracted with EtOAc (50 mL×2). The combined organic layers were washed with brine (100 mL), dried over sodium sulfate and concentrated in vacuum to give the title compound as a colorless oil (3.8 g, 65%).

후처리

  1. additionAfter the addition
  2. concentrationThe reaction mixture was carefully concentrated in vacuum
  3. customThe residue was separated between EtOAc (50 mL) and H2O (50 mL)
  4. extractionThe inorganic layer was extracted with EtOAc (50 mL×2)
  5. washThe combined organic layers were washed with brine (100 mL)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuum

출처 및 근거

ORD 기록
ord-590aea3f72994e058e45a7beef361d23
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916593B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트