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

Phenylacetic Acid → Benzeneacetamide, N-(2-acetylphenyl)-

HRID 364925
노트
인쇄 미리보기

반응식

HRID 364925 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:10])[CH3:9].[C:11]1([CH2:17][C:18](O)=[O:19])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl>[C:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:1][C:18](=[O:19])[CH2:17][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:10])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 999Phenylacetic AcidHCID 10868DicyclohexylcarbodiimideHCID 110862'-Aminoacetophenone

생성물 1

HCID 218938Benzeneacetamide, N-(2-acetylphenyl)-

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of o-aminoacetophenone (25 g.) and phenylacetic acid (25 g.) in anhydrous methylene dichloride (200 ml.) was prepared. To that mixture was added dicyclohexylcarbodiimide (40 g.) in portions of approx. 10 g. every 5 min. at ambient temperature. When the addition was completed the mixture was stirred for 4 hr. at ambient temperature. The mixture was then filtered, and the filtrate was evaporated in vacuo to dryness. The residue was crystallised from cyclohexane to give o-acetyl-N-(phenylacetyl)aniline, m.p. 78°.

후처리

  1. customwas prepared
  2. customevery 5 min.
  3. customat ambient temperature
  4. additionWhen the addition
  5. customat ambient temperature
  6. filtrationThe mixture was then filtered
  7. customthe filtrate was evaporated in vacuo to dryness
  8. customThe residue was crystallised from cyclohexane

출처 및 근거

ORD 기록
ord-c30de0092d444a9b9d4cc6dd5c8c2e66
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04607039

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트