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

Boron tribromide → HCID 59829751, 화합물

HRID 2223325
노트
인쇄 미리보기

반응식

HRID 2223325 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:19]C)=[C:6]([CH2:8][CH2:9][C:10]2[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:11]=2[C:12]#[N:13])[CH:7]=1.B(Br)(Br)Br>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:19])=[C:6]([CH2:8][CH2:9][C:10]2[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:11]=2[C:12]#[N:13])[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 22744933HCID 22744933, 화합물

생성물 1

HCID 59829751HCID 59829751, 화합물수율 81%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

A solution of 2-[2-(5-bromo-2-methoxyphenyl)-ethyl]-3-chlorobenzonitrile (0.187 g, 1.0 equiv) in CH2Cl2 (2.5 mL) was allowed to stir under an atmosphere of argon at −78° C. To this solution was added boron tribromide (1.0 M in CH2Cl2, 2.65 mL, 5.0 equiv). After 15 min at −78° C., the solution was allowed to warm to room temperature and stir overnight. The reaction was quenched by the addition of water and the solution was extracted with EtOAc. The organic phase was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromotagraphy (SiO2, 20% EtOAc in hexane) to give 2-[2-(5-bromo-2-hydroxyphenyl)-ethyl]-3-chlorobenzonitrile (0.144 g, 81%).

후처리

  1. temperatureto warm to room temperature
  2. stirringstir overnight
  3. customThe reaction was quenched by the addition of water
  4. extractionthe solution was extracted with EtOAc
  5. dry with materialThe organic phase was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by column chromotagraphy (SiO2, 20% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-b08aaa0274f54632bb51220a2cbc67ea
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07375125B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트