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

Water → 3-(3-Chlorophenyl)propionaldehyde

HRID 843573
노트
인쇄 미리보기

반응식

HRID 843573 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[CH2:6].[CH2:10](Cl)Cl.[OH2:13]>FC(F)(F)C(O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][CH2:6][CH:10]=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6344DichloromethaneHCID 14905m-Chlorostyrene

생성물 1

HCID 104195793-(3-Chlorophenyl)propionaldehyde

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To a 25° C. solution of 3-chlorostyrene in anhydrous CH2Cl2 ( 10.0 g, 72.15 mmol) was added a well-stirred solution of Pb(OAc)4 (35.2 g, 79.4 mmol) in trifluoroacetic acid (150 mL), dropwise. Reaction was completed within 30 minutes of the addition and after being stirred for a further 30 minutes, the mixture was poured into water, extracted with ether (3×), the combined organic layers were washed with saturated NaHCO3 solution, water, dried (MgSO4), and concentrated to a volume of about 15 mL and immediately used for the following reaction described below.

후처리

  1. customReaction
  2. additionwas completed within 30 minutes of the addition
  3. extractionextracted with ether (3×)
  4. washthe combined organic layers were washed with saturated NaHCO3 solution, water
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated to a volume of about 15 mL
  7. customimmediately used for the following reaction

출처 및 근거

ORD 기록
ord-80ae57e962354b54b94b849c380ee04b
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06380178B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트