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

Sodium Carbonate → HCID 86637901, 화합물

HRID 2389329
노트
인쇄 미리보기

반응식

HRID 2389329 반응식
Br[C:2]1[N:7]=[C:6]([CH2:8][OH:9])[CH:5]=[CH:4][CH:3]=1.CC1(C)C(C)(C)OB([C:18]2[CH:19]=[C:20]([CH:28]=[CH:29][CH:30]=2)[O:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])O1.C([O-])([O-])=O.[Na+].[Na+]>COCCOC>[OH:9][CH2:8][C:6]1[N:7]=[C:2]([C:18]2[CH:19]=[C:20]([CH:28]=[CH:29][CH:30]=2)[O:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH:3]=[CH:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 3517811(6-Bromopyridin-2-yl)methanolHCID 17749919Ethyl 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate

생성물 1

HCID 86637901HCID 86637901, 화합물수율 26.4%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

To a solution of (6-bromopyridin-2-yl)methanol (811 mg) in DME (20 mL) was added Pd(PPh3) 4 (453 mg) at ambient temperature under N2 gas atmosphere. After stirring for 20 minutes, ethyl [3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetate (1.20 g) and a solution of 2M Na2CO3 aqueous solution (5.88 mL) were added and the mixture was refluxed for 7 hours. The mixture was cooled to ambient temperature and partitioned between EtOAc (40 mL) and water. The organic layer was washed with saturated NaHCO3 aqueous solution, water and then brine, dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=10:1) to give ethyl {3-[6-(hydroxymethyl)pyridin-2-yl]phenoxy}acetate (297 mg) as a colorless oil.

후처리

  1. temperaturethe mixture was refluxed for 7 hours
  2. custompartitioned between EtOAc (40 mL) and water
  3. washThe organic layer was washed with saturated NaHCO3 aqueous solution, water
  4. dry with materialbrine, dried over anhydrous MgSO4
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customThe residue was purified by silica gel column chromatography (n-hexane:EtOAc=10:1)

출처 및 근거

ORD 기록
ord-f8e84e4ec76f42ef96b11402894e017b
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273745B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트