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

Trifluoroacetic acid → HCID 59215820, 화합물

HRID 421179
노트
인쇄 미리보기

반응식

HRID 421179 반응식
COC(=O)[CH2:4][NH:5][CH2:6][C@H:7]1[CH2:11][CH2:10][CH2:9][N:8]1[C:12]([O:14]C(C)(C)C)=O.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:6]1[NH:5][CH2:4][C:12](=[O:14])[N:8]2[CH2:9][CH2:10][CH2:11][C@H:7]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 59215855HCID 59215855, 화합물

생성물 1

HCID 59215820HCID 59215820, 화합물수율 99%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1,1-Dimethylethyl (2R)-2-({[2-(methyloxy)-2-oxoethyl]amino}methyl)-1-pyrrolidinecarboxylate (D3; 800 mg, 2.94 mmol) was dissolved in methylene chloride (10 ml) and treated with trifluoroacetic acid (2.5 ml) for 2 h. The reaction mixture was loaded as such on a SCX column and the non-basic compounds were washed away with methanol. The ninhydrine-positive fractions eluted with 1M methanolic ammonia were concentrated under vacuum at 40° C. for 30 min, isolating the title compound as a pale yellow oil: 410 mg, 2.92 mmol, 99% yield.

후처리

  1. washthe non-basic compounds were washed away with methanol
  2. washThe ninhydrine-positive fractions eluted with 1M methanolic ammonia
  3. concentrationwere concentrated under vacuum at 40° C. for 30 min

출처 및 근거

ORD 기록
ord-a3d0e22e87e14257ad35c62faa0265de
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097618B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트