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

Acetophenone → 1-Phenylethyl Acetate

HRID 1885069
노트
인쇄 미리보기

반응식

HRID 1885069 반응식
C(C1C=CC=CC=1)C.N([O:11][C:12](C)(C)[CH3:13])=O.ON1C(=O)C2=CC=CC=C2C1=O.C(=NO)(C1C=CC=CC=1)C.[N+](C(C1C=CC=CC=1)C)([O-])=O.[C:49]([C:52]1[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=1)(=[O:51])[CH3:50]>C(O)(=O)C>[C:12]([O:51][CH:49]([CH3:50])[C:52]1[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=1)(=[O:11])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 7410AcetophenoneHCID 7500EthylbenzeneHCID 10665N-HydroxyphthalimideHCID 10906Tert-Butyl nitriteHCID 236181-NitroethylbenzeneHCID 69185Acetophenonoxime

생성물 1

HCID 623411-Phenylethyl Acetate

시약·촉매·용매

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
1
HCID 176Acetic Acid용매

반응 조건

온도
80 °C

실험 절차

Ethylbenzene (1 ml), t-butyl nitrite (1 mmol), N-hydroxyphthalimide (0.2 mmol), and acetic acid (1 ml) were placed in a flask and were stirred at 80° C. in an atmosphere of argon gas (1 atm=0.101 MPa) for 20 hours. The resulting reaction mixture was analyzed to find that acetophenone oxime, (1-nitroethyl)benzene, acetophenone, and α-methylbenzyl acetate were formed in yields of 47%, 4%, 17%, and 14%, respectively.

후처리

  1. customThe resulting reaction mixture

출처 및 근거

ORD 기록
ord-75c12deac7154ec6a8aa7be5426cd2bf
출처 데이터셋
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06768023B2

반응 노트

불러오는 중…