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

Hydrochloric Acid → 4-(Fluoromethyl)benzoic acid

HRID 1794249
노트
인쇄 미리보기

반응식

HRID 1794249 반응식
[F:1][CH2:2][C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9]C)=[O:8])=[CH:5][CH:4]=1.[OH-].[Na+].Cl>CO>[F:1][CH2:2][C:3]1[CH:12]=[CH:11][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 21866613Methyl 4-(fluoromethyl)benzoate

생성물 1

HCID 139813684-(Fluoromethyl)benzoic acid수율 93.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To 200 ml of methanol, 8.68 g of methyl 4-(fluoromethyl)benzoate was dissolved, and 77 ml of aqueous solution of 1 N sodium hydroxide was added dropwise with stirring and cooling. The mixture was then stirred for 3.5 hours at room temperature. After the mixture was acidified with 1 N hydrochloric acid, the precipitated crystals were collected by filtration, and the filtrate was concentrated. The precipitated crystals were combined with the residue obtained by concentrating the filtrate, and water was added thereto. The mixture was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to provide 7.47 g of the objective compound as colorless crystals. M.p. 192–194° C.

후처리

  1. temperaturecooling
  2. stirringThe mixture was then stirred for 3.5 hours at room temperature
  3. filtrationthe precipitated crystals were collected by filtration
  4. concentrationthe filtrate was concentrated
  5. customobtained
  6. concentrationby concentrating the filtrate, and water
  7. additionwas added
  8. extractionThe mixture was extracted with ethyl acetate
  9. dry with materialdried over anhydrous magnesium sulfate
  10. distillationThe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-1a0b090fc7af426090a5af10d5d0e770
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07022723B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트