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

Sodium Bicarbonate → 4-Chloro-2-formylbenzoic acid

HRID 655829
노트
인쇄 미리보기

반응식

HRID 655829 반응식
[CH:1]([C:3]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:4]=1[C:5](NC)=[O:6])=[O:2].C(=O)([O-])[OH:15].[Na+]>Cl>[CH:1]([C:3]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:4]=1[C:5]([OH:15])=[O:6])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 577253672-formyl-4-chloro-N-methylbenzamide

생성물 1

HCID 110414214-Chloro-2-formylbenzoic acid

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of 2-formyl-4-chloro-N-methylbenzamide (3.19 g) and 10M hydrochloric acid (30 ml) was heated at reflux for 18 hours. The mixture was cooled and basified with saturated sodium hydrogen carbonate solution. The solution was then washed with ethyl acetate, then acidified with 2M hydrochloric acid. The product was extracted with ethyl acetate and the combined extracts dried with magnesium sulfate. The solution was then filtered and concentrated. This furnished 2-formyl-4-chlorobenzoic acid as a yellow solid (2.22 g, 75%); 1H NMR (400 MHz, CDCl3) δ 6.65 (0.5H, brs), 7.50 (2H, m), 7.65 (1H, m), 7.85 (0.5H, brm), 8.05 (1H, m).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 18 hours
  3. temperatureThe mixture was cooled
  4. washThe solution was then washed with ethyl acetate
  5. extractionThe product was extracted with ethyl acetate
  6. dry with materialthe combined extracts dried with magnesium sulfate
  7. filtrationThe solution was then filtered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-47d04d663d25480da1531e63c71b2b25
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071618B2

반응 노트

불러오는 중…