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

Bromide ion → 5-(Cyclopent-1-enyl)-2-methylpentan-2-ol

HRID 2187326
노트
인쇄 미리보기

반응식

HRID 2187326 반응식
[C:1]1([CH2:6][CH2:7][CH2:8][C:9](=[O:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1.[Br-].Cl.[CH2:14](OCC)C>>[C:1]1([CH2:6][CH2:7][CH2:8][C:9]([CH3:14])([OH:11])[CH3:10])[CH2:5][CH2:4][CH2:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 259Bromide ionHCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 135280095-(1-Cyclopentenyl)pentan-2-one

생성물 1

HCID 184338735-(Cyclopent-1-enyl)-2-methylpentan-2-ol수율 11%

실험 절차

5-(Cyclopent-1-enyl)-2-pentanone (5.95 g; 39 mmol) in ethyl ether (6 ml) was added dropwise to a 3M solution of methylnagnesium bromide in the same solvent (17 ml; 51 mmol) during 15 minutes. After 2 hours at reflux, the mixture was cooled down to room temperature, poured into ice (20 g), acidified with 5N HCl (20 ml) and extracted with MTBE (60 ml). The aqueous phase was separated and extracted again with MTBE (2×100 ml). The combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml), dried over MgSO4 and concentrated in vacuo. Bulb-to-bulb distillation (80° C./0.06 torr) yielded quantitatively 5.84 g of 5-(cyclopent-1-enyl)-2-methylpentan-2-ol containing 11% of 5-cyclopentylidene-2-methylpentan-2-ol.

후처리

  1. temperatureAfter 2 hours at reflux
  2. extractionextracted with MTBE (60 ml)
  3. customThe aqueous phase was separated
  4. extractionextracted again with MTBE (2×100 ml)
  5. washThe combined organic phases were washed with saturated NaHCO3 (80 ml), H2O (80 ml), brine (80 ml)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. distillationdistillation (80° C./0.06 torr)

출처 및 근거

ORD 기록
ord-13540fe1e8c841bc8238ffba1ff52f14
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410000B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트