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

Triacetoxyperiodinane → 3-(4-Phenylbutoxy)propionaldehyde

HRID 885529
노트
인쇄 미리보기

반응식

HRID 885529 반응식
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH2:14][OH:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>C(Cl)Cl>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH:14]=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 159087TriacetoxyperiodinaneHCID 672465283-(4-Phenylbutoxy)propan-1-ol

생성물 1

HCID 866583073-(4-Phenylbutoxy)propionaldehyde수율 58%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of Intermediate 12 (1.0 g, 4.8 mmol) in CH2Cl2 (20 mL) was added Dess-Martin periodinane (2.4 g, 5.76 mmol) and the reaction was stirred 2 hours at room temperature. The solution was then diluted with CH2Cl2 (40 mL), washed with water (2×20 mL), saturated solution of sodium bicarbonate (2×20 mL), and water (20 mL), dried (Na2SO4), and concentrated. The residue was purified by column chromatography (methylene chloride/acetone, 20:1) to afford the title compound (550 mg, 58%) as oil.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. washwashed with water (2×20 mL), saturated solution of sodium bicarbonate (2×20 mL), and water (20 mL)
  2. dry with materialdried (Na2SO4)
  3. concentrationconcentrated
  4. customThe residue was purified by column chromatography (methylene chloride/acetone, 20:1)

출처 및 근거

ORD 기록
ord-340ca6818a6448059668d22a17a67daa
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242177B2

반응 노트

불러오는 중…