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

Sodium Cyanide → 2,6-Diethyl-4-methylphenylacetonitrile

HRID 1890227
노트
인쇄 미리보기

반응식

HRID 1890227 반응식
[C-:1]#[N:2].[Na+].[CH2:4]([C:6]1[CH:13]=[C:12]([CH3:14])[CH:11]=[C:10]([CH2:15][CH3:16])[C:7]=1[CH2:8]Cl)[CH3:5]>O.C(#N)C>[CH2:4]([C:6]1[CH:13]=[C:12]([CH3:14])[CH:11]=[C:10]([CH2:15][CH3:16])[C:7]=1[CH2:8][C:1]#[N:2])[CH3:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8929Sodium CyanideHCID 667076972,6-Diethyl-4-methylbenzyl chloride

생성물 1

HCID 667077002,6-Diethyl-4-methylphenylacetonitrile수율 115.5%

시약·촉매·용매 2

HCID 962Water용매2회HCID 6342Acetonitrile용매2회

반응 조건

온도
75 °C

실험 절차

In a mixture of 50 g of water and 99 g of acetonitrile was dissolved 27.98 g of sodium cyanide. To this mixture, a solution of 157.18 g of 2,6-diethyl-4-methylbenzyl chloride (GC-area: 71%) in acetonitrile (293 g) was added dropwise at 75° C. over 2.5 hours. This mixture was stirred at 75° C. for 3 hours. To the reaction mixture was added 99 g of water, and the mixture was separated. The organic layer was concentrated. To the residue were added 99 g of water and 198 g of hexane and the mixture was separated. The organic layer was washed with 99 g of an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated to obtain 123.46 g of 2,6-diethyl-4-methylphenylacetonitrile (GC-area: 71%) as a brown oil.

후처리

  1. customthe mixture was separated
  2. concentrationThe organic layer was concentrated
  3. additionTo the residue were added 99 g of water and 198 g of hexane
  4. customthe mixture was separated
  5. washThe organic layer was washed with 99 g of an aqueous saturated sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b84433f24697484bbcd3de91fe4f3ff4
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507410B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트