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

Nitric Acid → HCID 22125091, 화합물

HRID 1858321
노트
인쇄 미리보기

반응식

HRID 1858321 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([NH:12][C:13](=[O:15])[CH3:14])([CH3:11])[CH3:10])=[CH:4][CH:3]=1.[N+:16]([O-])([OH:18])=[O:17]>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([NH:12][C:13](=[O:15])[CH3:14])([CH3:11])[CH3:10])=[CH:6][C:7]=1[N+:16]([O-:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 22124971HCID 22124971, 화합물

생성물 1

HCID 22125091HCID 22125091, 화합물수율 98%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

실험 절차

An ice-cooled solution of 3.3 g (12 mmol) of N-[2-(4-bromophenyl)-1,1-dimethylethyl]-acetamide in 3 ml of concentrated sulfuric acid was treated dropwise with a mixture of 3 ml of concentrated sulfuric acid and 6 ml of 90% nitric acid. After 1 hour the mixture was cautiously added to 200 ml of ice/water and the precipitated product extracted with 150 ml of dichloromethane. The organic solution was dried over magnesium sulfate, filtered and evaporated to give 3.7 g (98%) of N-[2-(4-bromo-3-nitrophenyl)-1,1-dimethyl-ethyl]acetamide as a white solid. [Mass spectrum (ESI) MH+ =315].

후처리

  1. extractionthe precipitated product extracted with 150 ml of dichloromethane
  2. dry with materialThe organic solution was dried over magnesium sulfate
  3. filtrationfiltered
  4. customevaporated

출처 및 근거

ORD 기록
ord-6bc287991fc74edd96cdd872060cb122
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06150373

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트