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

Diisobutylaluminum hydride → Tert-butyl 2-formyl-2-methylpyrrolidine-1-carboxylate

HRID 1619323
노트
인쇄 미리보기

반응식

HRID 1619323 반응식
[CH3:1][C:2]1([C:14](OC)=[O:15])[CH2:6][CH2:5][CH2:4][N:3]1[C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8].CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[CH:14]([C:2]1([CH3:1])[CH2:6][CH2:5][CH2:4][N:3]1[C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 235122231-Tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate

생성물 1

HCID 22456683Tert-butyl 2-formyl-2-methylpyrrolidine-1-carboxylate수율 98.4%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
-78 °C

실험 절차

To a solution of 1-tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate (3.5 g, 14.3 mmol) in toluene at −78° C. was added DIBAL-H (17.6 mL, 30 mmol, 1.7 M) dropwise, while maintaining the reaction temperature below −65° C. The reaction was stirred at −78° C. for 2 hr and then quenched with methanol (10 mL). The mixture was then diluted with ethyl acetate (50 mL), saturated NH4Cl was added and the mixture was stirred vigorously for 20 min at room temperature. The two phases were then separated and the aqueous layer was extracted with DCM (3×50 mL). The combined organics were then washed with brine, dried over Na2SO4, concentrated in vacuo and purified by column chromatography to give 3 g of the desired product.

후처리

  1. temperaturewhile maintaining the reaction temperature below −65° C
  2. customquenched with methanol (10 mL)
  3. additionThe mixture was then diluted with ethyl acetate (50 mL), saturated NH4Cl
  4. additionwas added
  5. stirringthe mixture was stirred vigorously for 20 min at room temperature
  6. customThe two phases were then separated
  7. extractionthe aqueous layer was extracted with DCM (3×50 mL)
  8. washThe combined organics were then washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated in vacuo
  11. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-8609296e573e472bb6ac5ef70c436f0d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772301B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트