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

Potassium Hydroxide → (2S)-2-amino-4-fluoro-4-methylpentan-1-ol

HRID 1009265
노트
인쇄 미리보기

반응식

HRID 1009265 반응식
[F:1][C:2]([CH3:11])([CH3:10])[CH2:3][C@H:4]1[CH2:8][O:7]C(=O)[NH:5]1.[OH-].[K+]>C(O)C>[NH2:5][C@@H:4]([CH2:3][C:2]([F:1])([CH3:11])[CH3:10])[CH2:8][OH:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 11194496(4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone

생성물 1

HCID 12167160(2S)-2-amino-4-fluoro-4-methylpentan-1-ol

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of the fluoro derivative (21.0 g) from Step 4 in 90% aqueous ethyl alcohol (216 μL) was added potassium hydroxide (21.9 g). The mixture was heated at reflux for 4 hours and cooled to room temperature. The mixture was then concentrated and co-evaporated with toluene (3×300 mL). The residue was dissolved in dichloromethane (500 mL) and stirred for 0.5 hour. The suspension was filtered through celite and the celite was washed with dichloromethane (3×100 mL). The filtrate was concentrated to dryness to yield (2S)-2-amino-4-fluoro-4-methylpentan-1-ol.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 hours
  3. concentrationThe mixture was then concentrated
  4. dissolutionThe residue was dissolved in dichloromethane (500 mL)
  5. filtrationThe suspension was filtered through celite
  6. washthe celite was washed with dichloromethane (3×100 mL)
  7. concentrationThe filtrate was concentrated to dryness

출처 및 근거

ORD 기록
ord-89830b8ffcb54425a68b9f11a8b635bd
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973037B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트