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

Water → (R)-3-hydroxy-1-phenylpyrrolidin-2-one

HRID 2261478
노트
인쇄 미리보기

반응식

HRID 2261478 반응식
[CH3:1][CH2:2][N:3]([CH:7]([CH3:9])C)[CH:4]([CH3:6])[CH3:5].S(OS(C(F)(F)F)(=O)=O)(C(F)(F)F)(=O)=[O:11].N1C[CH2:28][CH2:27][CH2:26]1.[OH2:30]>C(Cl)Cl>[OH:30][C@@H:9]1[CH2:1][CH2:2][N:3]([C:4]2[CH:5]=[CH:28][CH:27]=[CH:26][CH:6]=2)[C:7]1=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 31268PyrrolidineHCID 67749Trifluoromethanesulfonic anhydrideHCID 81531Diisopropylethylamine

생성물 1

HCID 59593452(R)-3-hydroxy-1-phenylpyrrolidin-2-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of alcohol (4.64 mmol) and DIEA (11.59 mmol) in DCM (10 mL) at −20° C. was added triflic anhydride (5.56 mmol) and the reaction mixture was stirred at this temperature for 20 min. A solution of pyrrolidine (3.86 mmol) in DCM (6 mL) was added and the reaction mixture was stirred at −20° C. for 1 hour. The reaction mixture was poured into water and extracted with EtOAc (3×). The combined organic extracts were washed with water (2×), brine, dried (Na2SO4) and evaporated to dryness. Purification by silica gel chromatography afforded the desired product.

후처리

  1. stirringthe reaction mixture was stirred at −20° C. for 1 hour
  2. extractionextracted with EtOAc (3×)
  3. washThe combined organic extracts were washed with water (2×), brine
  4. dry with materialdried (Na2SO4)
  5. customevaporated to dryness
  6. customPurification by silica gel chromatography

출처 및 근거

ORD 기록
ord-c262349734c3471fbdba3d59a7526958
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846954B2

반응 노트

불러오는 중…