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

Sodium Iodide → Methyl (S)-2-(Boc-amino)-4-iodobutanoate

HRID 1715636
노트
인쇄 미리보기

반응식

HRID 1715636 반응식
[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6]Br.[Na+].[I-:18]>CC(C)=O>[CH3:1][O:2][C:3](=[O:16])[C@@H:4]([NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:6][I:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 10685328Methyl (S)-2-(Boc-amino)-4-bromobutyrate

생성물 1

HCID 14394150Methyl (S)-2-(Boc-amino)-4-iodobutanoate수율 92%

시약·촉매·용매 1

HCID 180Acetone용매

반응 조건

온도
70 °C

실험 절차

A mixture of (S)-4-bromo-2-tert-butoxycarbonylaminobutyric acid methyl ester (1.19 g, 4.0 mmol) (Example 120, Steps A-D) and NaI (6.0 g, 40.0 mmol) in acetone (25 mL) was heated to 70° C. for 2 hours. The mixture was then cooled to room temperature, concentrated under reduced pressure and partitioned between water (10 mL) and ether (40 mL). The layers were separated and the organic layer was washed with water (10 mL), dried over MgSO4, filtered through Celite, and concentrated under reduced pressure to afford 1.26 g of the product (92% yield).

후처리

  1. temperatureThe mixture was then cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. custompartitioned between water (10 mL) and ether (40 mL)
  4. customThe layers were separated
  5. washthe organic layer was washed with water (10 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered through Celite
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-72608d66019440e6900203f19c2d1e8c
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07799782B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트