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

Hydrochloric Acid → 3-Fluoro-4-formylbenzoic acid

HRID 2233056
노트
인쇄 미리보기

반응식

HRID 2233056 반응식
Br[CH:2](Br)[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1[F:12].Cl.[OH2:15]>C(O)C.[N+]([O-])([O-])=O.[Ag+]>[F:12][C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:3]=1[CH:2]=[O:15])[C:7]([OH:9])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 592951004-(Dibromomethyl)-3-fluorobenzoic acid

생성물 1

HCID 212845583-Fluoro-4-formylbenzoic acid

시약·촉매·용매 2

HCID 24470Silver Nitrate촉매HCID 702Ethanol용매

실험 절차

AgNO3 (0.39 mol) in hot H2O (90 mL) is added dropwise to a solution of crude 4-dibromomethyl-3-fluorobenzoic acid (2, 0.19 mol) in ethanol (EtOH) (480 mL) at 50° C. over 10 min and then the mixture is stirred at the same temperature for 45 min. After cooling to room temperature, the mixture is poured into 1 N HCl (200 mL) and filtered off. The residue is washed with EtOH and the filtrate is concentrated to ca. 300 mL. The mixture is extracted twice with ethylacetate (EtOAc) and the combined organic layers are washed with brine, dried over MgSO4 and evaporated in vacuo. The crystals are collected by filtration and washed with ether/hexane (1:1) to give 3-fluoro-4-formyl benzoic acid (3).

후처리

  1. filtrationfiltered off
  2. washThe residue is washed with EtOH
  3. concentrationthe filtrate is concentrated to ca. 300 mL
  4. extractionThe mixture is extracted twice with ethylacetate (EtOAc)
  5. washthe combined organic layers are washed with brine
  6. dry with materialdried over MgSO4
  7. customevaporated in vacuo
  8. filtrationThe crystals are collected by filtration
  9. washwashed with ether/hexane (1:1)

출처 및 근거

ORD 기록
ord-692b60c9434f4ceea743837c05705718
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709470B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트