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

Sodium Carbonate → N-(1-propyl)-4-hydroxyphenylacetamide

HRID 326562
노트
인쇄 미리보기

반응식

HRID 326562 반응식
[CH2:1]([NH:4][C:5](=[O:17])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13]C(=O)C)=[CH:9][CH:8]=1)[CH2:2][CH3:3].C(=O)([O-])[O-].[Na+].[Na+]>CO.O>[CH2:1]([NH:4][C:5](=[O:17])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([OH:13])=[CH:11][CH:12]=1)[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 10340Sodium CarbonateHCID 15730061N-(1-propyl)-4-acetoxyphenylacetamide

생성물 1

HCID 10750308N-(1-propyl)-4-hydroxyphenylacetamide

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a solution of N-(1-propyl)-4-acetoxyphenylacetamide (11.4 g) in methanol (25 ml) was added a solution of sodium carbonate (2.65 g) in water (50 ml), and the mixture stirred overnight at ambient temperature. The methanol was removed in vacuo and the aqueous residue acidified to pH2. The product was extracted with ethyl acetate (3×50 ml), and the organic extracts combined and washed with brine (50 ml), dried (MgSO4). The solvent was evaporated to give N-(1-propyl)-4-hydroxyphenylacetamide as a yellow oil, essentially pure by TLC, NMR: 0.85(t,3H, CH3), 1.3-1.6(m,2H, CH2CH3), 3.15(t,2H, CH2N), 3.5(s,2H, CH2Ar), 5.75 (broad t,1H, NH), 6.85(d,2H, phenyl-H), 7.05(d,2H, phenyl-H) (the spectrum also contained peaks due to ethyl acetate); m/e 194 (M+H)+.

후처리

  1. customThe methanol was removed in vacuo
  2. extractionThe product was extracted with ethyl acetate (3×50 ml)
  3. washwashed with brine (50 ml)
  4. dry with materialdried (MgSO4)
  5. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-5ba1de494b3d440eb1fa3c2e0865d181
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05270311

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트