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

Water → (2,6-Diisopropylphenyl)[1-(2'-methoxybiphenyl-3-yl)ethylidene]amine

HRID 45478
노트
인쇄 미리보기

반응식

HRID 45478 반응식
Br[C:2]1[CH:3]=[C:4]([C:8](=[N:10][C:11]2[C:16]([CH:17]([CH3:19])[CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=2[CH:20]([CH3:22])[CH3:21])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[Li]CCCC.Br[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[O:35][CH3:36].O>C1COCC1.[Cl-].[Cl-].[Zn+2].CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C>[CH:20]([C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([CH:17]([CH3:19])[CH3:18])[C:11]=1[N:10]=[C:8]([C:4]1[CH:3]=[C:2]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[O:35][CH3:36])[CH:7]=[CH:6][CH:5]=1)[CH3:9])([CH3:22])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 962WaterHCID 113582-BromoanisoleHCID 58238584N-[1-(3-Bromophenyl)ethylidene]-2,6-diisopropylanilineHCID 178418339Butyllithium

생성물 1

HCID 58238573(2,6-Diisopropylphenyl)[1-(2'-methoxybiphenyl-3-yl)ethylidene]amine수율 79%

시약·촉매·용매 3

HCID 3007855
Zincchloride
촉매
HCID 178418851HCID 178418851, 화합물촉매
HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-70 °C

실험 절차

To a solution of 2.78 g (7.75 mmol) of 13 in 30 mL of THF, 3.10 mL (7.75 mmol) of 2.5 M nBuLi in hexanes was added at −100° C. The reaction mixture was stirred for 1 hr at −70° C., then cooled to −100° C., and 8.35 mL (8.35 mmol) of 1M ZnCl2 in THF was added. The resulting mixture was slowly warmed to room temperature, stirred for 12 hr at this temperature, and then 1.45 g (7.75 mmol) of 2-bromoanisole and 85 mg (0.15 mmol) of Pd(PtBu3)2 were added. The resulting mixture was refluxed for 3 hr, and then 5 mL of water was added. This mixture was passed through short layer of silica gel 60 (40-63 um) which was then additionally washed with 30 mL of dichloromethane. The combined organic filtrate was evaporated to dryness, and the product was isolated by flash chromatography on silica gel 60(40-63 um, eluent: from hexanes to hexanes-diethyl ether=20:1, vol.). This procedure gave 2.36 g (79%) of the title product.

후처리

  1. temperaturecooled to −100° C.
  2. temperatureThe resulting mixture was slowly warmed to room temperature
  3. stirringstirred for 12 hr at this temperature
  4. temperatureThe resulting mixture was refluxed for 3 hr
  5. washwas then additionally washed with 30 mL of dichloromethane
  6. customThe combined organic filtrate was evaporated to dryness
  7. customthe product was isolated by flash chromatography on silica gel 60(40-63 um, eluent: from hexanes to hexanes-diethyl ether=20:1, vol.)

출처 및 근거

ORD 기록
ord-48ce2117ca204564bb083007c42e29cc
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541522B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트