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

Ammonia → HCID 54274160, 화합물

HRID 1416523
노트
인쇄 미리보기

반응식

HRID 1416523 반응식
[CH:1]([C:3]12[CH2:9][N:6]3[CH2:7][CH:8]1[CH:4]2[CH2:5]3)=O.[C-:10]#[N:11].[K+].[NH3:13].[Cl-].[NH4+]>O>[NH2:13][CH:1]([C:3]12[CH2:9][N:6]3[CH2:7][CH:8]1[CH:4]2[CH2:5]3)[C:10]#[N:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 9032Potassium CyanideHCID 25517Ammonium ChlorideHCID 450871594-Azatricyclo[2.2.1.0~2,6~]heptane-1-carbaldehyde

생성물 1

HCID 54274160HCID 54274160, 화합물수율 58%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To an icecooled solution of 1-formyl-4-azatricyclo[2.2.1.02,6 ]heptane (3.56 g, 29 mmol) in water (5 ml) was added a solution of potassium cyanide (2.08 g, 31.9 mmol) in water (5 ml) over 30 min. After an additional 1 h, cooling was removed and the reaction stirred at room temperature for 16 h. The cyanohydrin product was then added 25% aqueous ammonia (4.0 ml, 52 mmol) and ammonium chloride (7.76 g, 145 mmol). The reaction mixture was stirred at room temperature for 18 h and then extracted with isopropanole/dichloromethane (1:10) (10×75 ml). The organic phases were dried and evaporated to give the title compound as an oil (2.5 g, 58%).

후처리

  1. temperaturecooling
  2. customwas removed
  3. stirringThe reaction mixture was stirred at room temperature for 18 h
  4. extractionextracted with isopropanole/dichloromethane (1:10) (10×75 ml)
  5. customThe organic phases were dried
  6. customevaporated

출처 및 근거

ORD 기록
ord-cc9378448944404c835f9c103736cf34
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05914338

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트