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

Hydrochloric Acid → 2-((3,5-Dichloro-2-cyanobenzyl)oxy)ethyl acetate

HRID 1051951
노트
인쇄 미리보기

반응식

HRID 1051951 반응식
Br[CH2:2][C:3]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]([Cl:12])[C:4]=1[C:5]#[N:6].[C:13]([O:16][CH2:17][CH2:18][OH:19])(=[O:15])[CH3:14].[H-].[Na+].Cl>C1COCC1>[C:13]([O:16][CH2:17][CH2:18][O:19][CH2:2][C:3]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]([Cl:12])[C:4]=1[C:5]#[N:6])(=[O:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 10960Glycol monoacetateHCID 24758Sodium hydrideHCID 897049972-(Bromomethyl)-4,6-dichlorobenzonitrile

생성물 1

HCID 897048262-((3,5-Dichloro-2-cyanobenzyl)oxy)ethyl acetate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a soln. of 2-(bromomethyl)-4,6-dichlorobenzonitrile (1.3 mmol) (A.2.2.1.) and 2-hydroxyethyl acetate (1.43 mmol) in 7 mL THF was added NaH (1.95 mmol, 60% suspension in oil). The reaction mixture was stirred at RT overnight and then poured into a 1M HCl soln. The mixture was extracted twice with EtOAc. The comb. org. layers were washed with brine, dried over MgSO4 and conc. in vacuo. Purification with CC (0-25% EtOAc/Hept) gives the desired compound as orange oil.

후처리

  1. extractionThe mixture was extracted twice with EtOAc
  2. washlayers were washed with brine
  3. dry with materialdried over MgSO4 and conc. in vacuo
  4. customPurification with CC (0-25% EtOAc/Hept)

출처 및 근거

ORD 기록
ord-d5630ada16484f649a587c07ff98d1b0
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388197B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트