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

Benzyltrimethylammonium hydroxide → HCID 178510368, 화합물

HRID 450858
노트
인쇄 미리보기

반응식

HRID 450858 반응식
[Na].CO[CH:4](OC)[C:5](=[CH:8]O)[C:6]#[N:7].[C:12]([CH2:14][C:15](=[S:17])[NH2:16])#[N:13].[OH-].C([N+](C)(C)C)C1C=CC=CC=1>Cl.C(N(CC)CC)C>[C:12]([C:14]1[C:15]([SH:17])=[N:16][CH:4]=[C:5]([C:6]#[N:7])[CH:8]=1)#[N:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 66854Benzyltrimethylammonium hydroxideHCID 14162772-CyanoethanethioamideHCID 5360545SodiumHCID 579371032-Dimethoxymethyl-3-hydroxy-acrylonitrile

생성물 1

HCID 178510368HCID 178510368, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매2회
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8471
Triethylamine
용매

반응 조건

온도
50 °C

실험 절차

A suspension of the sodium salt of 2-dimethoxymethyl-3-hydroxy-acrylonitrile (3.94 g, 23.86 mmol) in hydrochloric acid (20 ml, 0.5 M) is heated at 50° C. for 30 minutes. Excess hydrochloric acid is neturalized using triethylamine, before adding cyanoacetothioamide (2.39 g, 23.9 mmol) and a catalytic amound of benzyltrimethylammonium hydroxide. The mixture is stirred at room temperature for two hours, heated at 60° C. for 2 hours and then refluxed for 4 hours. Evaporation of the solvents leaves a solid that is purified on silicagel to yield 3,5-dicyano-2-marcaptopyridine.

후처리

  1. temperatureheated at 60° C. for 2 hours
  2. temperaturerefluxed for 4 hours
  3. customEvaporation of the solvents
  4. customleaves a solid
  5. customthat is purified on silicagel
  6. customto yield 3,5-dicyano-2-marcaptopyridine

출처 및 근거

ORD 기록
ord-0704176d76584d41a772a9f45bc0554a
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08486996B2

반응 노트

불러오는 중…