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

Acetonitrile → 5-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran

HRID 1850371
노트
인쇄 미리보기

반응식

HRID 1850371 반응식
[Br:1]N1C(=O)CCC1=O.C(#N)C.[CH3:12][C:13]1([CH3:25])[CH2:17][C:16]2[C:18]([CH3:24])=[CH:19][C:20]([CH3:23])=[C:21]([CH3:22])[C:15]=2[O:14]1>O>[Br:1][C:19]1[C:20]([CH3:23])=[C:21]([CH3:22])[C:15]2[O:14][C:13]([CH3:25])([CH3:12])[CH2:17][C:16]=2[C:18]=1[CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6342AcetonitrileHCID 67184N-bromobutanimideHCID 117454372,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran

생성물 1

HCID 667609285-Bromo-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran수율 86%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

N-bromosuccinimide (12.5 g, 70.0 mmol) was added to a solution of acetonitrile (165 mL) containing 2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran (11.1 g, 58.3 mmol) synthesized in Reference Example 3 under ice-cooling condition, and the mixture was warmed to room temperature. After stirring for 5 hours, water was added to the reaction solution. The generated precipitate was collected by filtration and washed with a mixture of acetonitrile/water (1/2). The solid was dried to give 13.5 g of the title compound (yield: 86%).

후처리

  1. customsynthesized in Reference Example 3 under ice-
  2. temperaturecooling condition
  3. filtrationThe generated precipitate was collected by filtration
  4. washwashed with a mixture of acetonitrile/water (1/2)
  5. customThe solid was dried

출처 및 근거

ORD 기록
ord-68e6d64275b441dc99a0b8d2cc5cc951
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08957069B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트