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

Benzyl Chloride → (2,5-Dimethyl-3-nitrophenyl)-benzyl ether

HRID 426838
노트
인쇄 미리보기

반응식

HRID 426838 반응식
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([CH3:11])=[CH:4][C:3]=1[OH:12].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Cl)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>CN(C)C=O>[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([CH3:11])=[CH:4][C:3]=1[O:12][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7503Benzyl ChlorideHCID 11430Potassium CarbonateHCID 189815232,5-Dimethyl-3-nitrophenol

생성물 1

HCID 20390195(2,5-Dimethyl-3-nitrophenyl)-benzyl ether

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 433 g. 2,5-dimethyl-3-nitrophenol, 360 g. potassium carbonate, 326 ml. benzyl chloride and 2 liters dimethyl formamide is stirred overnight at 50° C. The reaction mixture is then filtered with suction and the filtrate is evaporated to dryness in a vacuum. The residue is poured on to 4 liters of ice-water and, after suction filtration and drying in the air, there are obtained 668 g. of yellowish crystals; m.p. 66°-68° C.

후처리

  1. additionA mixture of 433 g
  2. filtrationThe reaction mixture is then filtered with suction
  3. customthe filtrate is evaporated to dryness in a vacuum
  4. additionThe residue is poured on to 4 liters of ice-water
  5. filtrationafter suction filtration
  6. customdrying in the air, there
  7. customare obtained 668 g

출처 및 근거

ORD 기록
ord-b94e3064a0a14acbbb967ee7ae03b2c1
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04171446

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트