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

Formaldehyde → 5-(Dimethylamino)-2-methoxyphenol

HRID 1789761
노트
인쇄 미리보기

반응식

HRID 1789761 반응식
N[C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1.[CH2:11]=O.[C:13]([BH3-])#[N:14].[Na+].[H-]>C(O)C.C(O)(=O)C>[CH3:11][N:14]([CH3:13])[C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 712FormaldehydeHCID 743145-Amino-2-methoxyphenolHCID 166653HydrideHCID 5003444Sodium cyanoborohydride

생성물 1

HCID 220363245-(Dimethylamino)-2-methoxyphenol수율 20%

시약·촉매·용매 2

HCID 176Acetic Acid용매
HCID 702
Ethanol
용매

실험 절차

To a stirred solution of 5-amino-2-methoxyphenol (5.0 g, 36 mmol) in ethanol (250 mL), was added 33% formaldehyde (4×1.5 mL at times 0, 60 min, 140 min and 185 min) and sodium cyanoborohydride (4×0.8 g, at times 30 min, 120 min, 165 min and 210 min). After each addition of the hydride, pH was adjusted to ˜6 using acetic acid. The mixture was stirred for an additional 2 h and then concentrated in vacuo. The residue was partitioned between brine/diethyl ether and the organic phase was dried and concentrated. The residue was purified by column chromatography on silica gel using hexane/EtOAc (7:3) as eluent to give 1.17 g (20%) of the title compound. MS m/z 168 (M+H)+.

후처리

  1. concentrationconcentrated in vacuo
  2. customThe residue was partitioned between brine/diethyl ether
  3. customthe organic phase was dried
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-d018fec252db4e5a9e88142adb2f4a73
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07071180B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트