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

Sulfuric Acid → Tert-butyl octahydro-1H-indole-2-carboxylate

HRID 917797
노트
인쇄 미리보기

반응식

HRID 917797 반응식
[NH:1]1[CH:9]2[CH:4]([CH2:5][CH2:6][CH2:7][CH2:8]2)[CH2:3][CH:2]1[C:10]([OH:12])=[O:11].OS(O)(=O)=O>C(Cl)(Cl)Cl>[C:4]([O:11][C:10]([CH:2]1[CH2:3][CH:4]2[CH:9]([CH2:8][CH2:7][CH2:6][CH2:5]2)[NH:1]1)=[O:12])([CH3:9])([CH3:5])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 3274680Octahydroindole-2-carboxylic acid

생성물 1

HCID 13308983Tert-butyl octahydro-1H-indole-2-carboxylate수율 200%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

Octahydro-indole-2-carboxylic acid 11b (5.0 g, 29.5 mmol, purchased from Bachem) was suspended in 200 mL of CHCl3 then cooled in a dry ice/acetone bath. H2SO4 (120 uL/mmol) was added followed by bubbling in excess isobutylene. The mixture was sealed and the ice bath removed. The mixture was stirred at RT for 12 hours. The reaction mixture was carefully unsealed after cooling and concentrated. EtOAc was added and washed with saturated sodium bicarbonate soln, brine, dried over sodium sulfate, then filtered and concentrated to give octahydro-indole-2-carboxylic acid tert-butyl ester 12b (6.65 g, 29.5 mmol, 100%).

후처리

  1. temperaturethen cooled in a dry ice/acetone bath
  2. customby bubbling in excess isobutylene
  3. customThe mixture was sealed
  4. customthe ice bath removed
  5. temperatureafter cooling
  6. concentrationconcentrated
  7. additionEtOAc was added
  8. washwashed with saturated sodium bicarbonate soln
  9. dry with materialbrine, dried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-478737160a0b4107b08f5ffedda8b0ce
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07273885B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트