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

(3-Isopropyl-2-propoxyphenyl)methanol → 3-Isopropyl-2-propoxybenzaldehyde

HRID 2097029
노트
인쇄 미리보기

반응식

HRID 2097029 반응식
[CH:1]([C:4]1[C:5]([O:12][CH2:13][CH2:14][CH3:15])=[C:6]([CH2:10][OH:11])[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2]>C1C=CC=CC=1.O=[Mn]=O>[CH:1]([C:4]1[C:5]([O:12][CH2:13][CH2:14][CH3:15])=[C:6]([CH:7]=[CH:8][CH:9]=1)[CH:10]=[O:11])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 59277603(3-Isopropyl-2-propoxyphenyl)methanol

생성물 1

HCID 592776233-Isopropyl-2-propoxybenzaldehyde수율 54.7%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 241Benzene용매

실험 절차

MnO2 (6.88 g, 79.2 mmol) was added to a stirring solution of (3-isopropyl-2-propoxyphenyl)methanol (2.75 g, 13.2 mmol) in benzene (130 mL) under N2. After stirring for 48 h, the solution was filtered over diatomaceous earth, the pad rinsed with CH2Cl2 (200 mL) and the solution concentrated to a yellow oil. Purification by column chromatography (silica gel, hexanes/EtOAc, 100 to 98:2) gave the title compound (1.49 g, 54%) as a light yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 10.26 (s, 1H), 7.67 (dd, J=7.6, 1.7 Hz, 1H), 7.59 (dd, J=7.6, 1.7 Hz, 1H), 7.28 (t, J=7.6 Hz, 1H), 3.87 (t, J=6.4 Hz, 2H), 3.35-3.30 (m, 2H), 1.85-1.78 (m, 2H), 1.21 (t, J=6.9 Hz, 7H), 1.03 (t, J=7.3 Hz, 3H).

후처리

  1. filtrationthe solution was filtered over diatomaceous earth
  2. washthe pad rinsed with CH2Cl2 (200 mL)
  3. concentrationthe solution concentrated to a yellow oil
  4. customPurification by column chromatography (silica gel, hexanes/EtOAc, 100 to 98:2)

출처 및 근거

ORD 기록
ord-80b2787469d64294a5816fd117d0b7ca
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450307B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트