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

Hydrochloric Acid → 2,2-Dimethylcyclopentane-1-carbonitrile

HRID 1168618
노트
인쇄 미리보기

반응식

HRID 1168618 반응식
S([CH2:11][N+:12]#[C-])(C1C=CC(C)=CC=1)(=O)=O.CC(C)([O-])C.[K+].[CH3:20][C:21]1([CH3:27])[CH2:25][CH2:24][CH2:23][C:22]1=O.Cl>CS(C)=O.CO.C(OCC)(=O)C>[CH3:20][C:21]1([CH3:27])[CH2:25][CH2:24][CH2:23][CH:22]1[C:11]#[N:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 1382862,2-DimethylcyclopentanoneHCID 161915Tosylmethyl isocyanideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 100574962,2-Dimethylcyclopentane-1-carbonitrile수율 31%

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide
용매
HCID 887Methanol용매
HCID 8857Ethyl Acetate용매

반응 조건

온도
0 °C

실험 절차

Tosylmethyl isocyanide (3.76 g, 19.3 mmol) was dissolved in dimethylsulfoxide (15 mL) and cooled to 0° C. Solid potassium t-butoxide (6.3 g, 59.2 mmol) was added and a thick brown precipitate formed. The reaction mixture was warmed to room temperature and 2,2-dimethylcyclopentanone (2.0 mL, 16.0 mmol) was added in anhydrous methanol (680 μL) and the reaction mixture was stirred for 30 hours. It was diluted with ethyl acetate, acidified with hydrochloric acid and extracted with hexanes. The extracts were dried over magnesium sulfate, filtered and the solvent was removed to provide a brown oil which was purified by chromatography on silica gel eluted with 0-50% dichloromethane in hexanes to yield a yellow oil (612 mg, 31%).

후처리

  1. customa thick brown precipitate formed
  2. temperatureThe reaction mixture was warmed to room temperature
  3. extractionextracted with hexanes
  4. dry with materialThe extracts were dried over magnesium sulfate
  5. filtrationfiltered
  6. customthe solvent was removed
  7. customto provide a brown oil which
  8. customwas purified by chromatography on silica gel
  9. washeluted with 0-50% dichloromethane in hexanes

출처 및 근거

ORD 기록
ord-19a1f69ddc1c462ea97473e6666a72ac
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06624309B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트