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

Sodium Azide → (S)-5-(2-azido-ethyl)-2,2,4,4-tetramethyl-[1,3]dioxolane

HRID 1807061
노트
인쇄 미리보기

반응식

HRID 1807061 반응식
[CH3:1][C:2]1([CH3:16])[O:6][C@@H:5]([CH2:7][CH2:8]OS(C)(=O)=O)[C:4]([CH3:15])([CH3:14])[O:3]1.[N-:17]=[N+:18]=[N-:19].[Na+]>CN(C)C=O>[N:17]([CH2:8][CH2:7][C@@H:5]1[O:6][C:2]([CH3:16])([CH3:1])[O:3][C:4]1([CH3:15])[CH3:14])=[N+:18]=[N-:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 86640453methanesulfonic acid 2-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-ethyl ester

생성물 1

HCID 86640454(S)-5-(2-azido-ethyl)-2,2,4,4-tetramethyl-[1,3]dioxolane수율 81.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
95 °C

실험 절차

Step H To a solution of methanesulfonic acid 2-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-ethyl ester (2.5 g, 9.9 mmol) in N,N-dimethylformamide (50 mL) was added NaN3 (6 g, 70 mmol). The reaction mixture was heated at 95° C. for 4 h. Then the mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine several times, dried over MgSO4, concentrated to give (S)-5-(2-azido-ethyl)-2,2,4,4-tetramethyl-[1,3]dioxolane as a yellow oil (1.6 g, 80%).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThen the mixture was partitioned between ethyl acetate and water
  2. customThe organic layer was separated
  3. washwashed with water, brine several times
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-018630b73eee41abacd1db14ac765373
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354444B2

반응 노트

불러오는 중…