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

Cycloheptanone → 1-Oxaspiro(2.6)nonane

HRID 1778892
노트
인쇄 미리보기

반응식

HRID 1778892 반응식
[I-].C[S+](C)C.[C:6]1(=[O:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[CH3:14]C(C)([O-])C.[K+]>CS(C)=O>[O:13]1[C:6]2([CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)[CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10400CycloheptanoneHCID 75127Trimethylsulfonium iodideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 6429411-Oxaspiro(2.6)nonane

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

To a mixture of trimethylsulfonium iodide (35.7 g) in 300 mL dry DMSO was added 11.2 g of cycloheptanone with stirring. A solution of potassium tert-butoxide (16.83 g) in 200 mL dry DMSO was slowly added. The resulting solution was stirred at room temperature for 16 hours. The reaction mixture was quenched by addition of water (600 mL), and extracted with diethyl ether (3×200 mL). The combined organic layers were washed with water (200 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure to give the product.

후처리

  1. stirringThe resulting solution was stirred at room temperature for 16 hours
  2. customThe reaction mixture was quenched by addition of water (600 mL)
  3. extractionextracted with diethyl ether (3×200 mL)
  4. washThe combined organic layers were washed with water (200 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto give the product

출처 및 근거

ORD 기록
ord-988589e00877493eb98baf48cf2a1bfe
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266877B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트