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

Potassium Bromide → tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate

HRID 1427723
노트
인쇄 미리보기

반응식

HRID 1427723 반응식
[C:1]([N:8]1[CH2:12][CH2:11][C@@H:10]([CH2:13][OH:14])[CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CC1(C)N([O])C(C)(C)CCC1.[Br-].[K+].[O-]Cl.[Na+].C([O-])(O)=O.[Na+]>C(Cl)Cl.O>[C:4]([O:3][C:1]([N:8]1[CH2:12][CH2:11][C@@H:10]([CH:13]=[O:14])[CH2:9]1)=[O:2])([CH3:7])([CH3:6])[CH3:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 253877Potassium BromideHCID 516892Sodium BicarbonateHCID 1514340tert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 2724126TempoHCID 23665760Sodium Hypochlorite

생성물 1

HCID 1514342tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate수율 87%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

반응 조건

온도
5 °C

실험 절차

To a solution of (R)-Boc-3-pyrrolidinemethanol (5.0 g, 24.8 mmol) in DCM was added TEMPO (80 mg, 0.5 mmol) and potassium bromide (150 mg, 1.3 mmol). This mixture was cooled to 5° C. and vigorously stirred as a pre-chilled (at 0° C.) 1:1 mixture of NaOCl in water (53 mL) and a saturated, aqueous NaHCO3 solution (53 mL) was added dropwise. The resultant mixture was extracted with DCM (3×50 mL). The combined organic layers were washed with water (50 mL) and saturated aqueous NaCl (50 mL). The organic layer was dried over anhydrous Na2SO4 to yield 4.3 g of the title compound, which was used without further purification.

후처리

  1. temperaturea pre-chilled
  2. extractionThe resultant mixture was extracted with DCM (3×50 mL)
  3. washThe combined organic layers were washed with water (50 mL) and saturated aqueous NaCl (50 mL)
  4. dry with materialThe organic layer was dried over anhydrous Na2SO4

출처 및 근거

ORD 기록
ord-0b3d24b9cf6a4701b6cdad70ff75fdaf
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933249B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트