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

Iodine → 2-Fluoro-6-iodo-4-methylaniline

HRID 400599
노트
인쇄 미리보기

반응식

HRID 400599 반응식
[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[NH2:9].[I:10]I>CO.OO>[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([I:10])[C:3]=1[NH2:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 807IodineHCID 679842-Fluoro-4-methylaniline

생성물 1

HCID 109779002-Fluoro-6-iodo-4-methylaniline수율 87.6%

시약·촉매·용매 2

HCID 784Hydrogen Peroxide용매HCID 887Methanol용매2회

실험 절차

A solution of 2-fluoro-4-methylphenylamine (1.25 g, 10 mmol) in 5 mL of methanol was treated with a solution of iodine (1.27 g, 5 mmol) in a mixture of 25 mL of methanol and 3 mL of hydrogen peroxide over a period of 15 minutes at room temperature. After 18 hours, the reaction mixture was quenched with 30 mL of saturated aqueous sodium thiosulfate and extracted with three 50 mL portions of dichloromethane. The combined organic layers were washed with two 30 mL portions of saturated sodium bisulfite solution, three 50 mL portions of water, dried over sodium sulfate, and concentrated in vacuo. Chromatography on SiO2 (10% ethyl acetate in hexanes) gave 1.1 g of the title product as a light brownish oil (44% yield).

후처리

  1. customthe reaction mixture was quenched with 30 mL of saturated aqueous sodium thiosulfate
  2. extractionextracted with three 50 mL portions of dichloromethane
  3. washThe combined organic layers were washed with two 30 mL portions of saturated sodium bisulfite solution, three 50 mL portions of water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f2188e324455469d907cc77fb48a578e
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08741897B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트